PUBLICACIONES PERIODO 2019 – 2015

2019

Hurst, G.A., Slootweg, J.C., Balu, A.M., Climent-Bellido, M.S., Gomera, A., Gomez, P., Luque, R., Mammino, L., Spanevello, R.A., Saito, K., Ibanez, J.G. International Perspectives on Green and Sustainable Chemistry Education via Systems Thinking (2019) Journal of Chemical Education, 96 (12), pp. 2794-2804 https://doi.org/10.1021/acs.jchemed.9b00341

Perez Mora, B., Bellú, S., Mangiameli, M.F., Frascaroli, M.I., González, J.C. Response surface methodology and optimization of arsenic continuous sorption process from contaminated water using chitosan (2019) Journal of Water Process Engineering, 32, art. no. 100913 https://doi.org/10.1016/j.jwpe.2019.100913

Martínez Bilesio, A.R., Batistelli, M., García-Reiriz, A.G.Fusing data of different orders for environmental monitoring (2019) Analytica Chimica Acta, 1085, pp. 48-60 https://doi.org/10.1016/j.aca.2019.08.005

 

Rodrigues, D.R., Olivieri, A.C., Fragoso, W.D., Lemos, S.G. Complex numbers-partial least-squares applied to the treatment of electrochemical impedance spectroscopy data (2019) Analytica Chimica Acta, 1080, pp. 1-11 https://doi.org/10.1016/j.aca.2019.07.047

 

Olivieri, A.C., Escandar, G.M. Analytical chemistry assisted by multi-way calibration: A contribution to green chemistry (2019) Talanta, 204, pp. 700-712 https://doi.org/10.1016/j.talanta.2019.06.022  

 

Pellegrino Vidal, R.B., Olivieri, A.C. Contribution to second-order calibration based on multivariate curve resolution with and without previous chromatographic synchronization (2019) Analytica Chimica Acta, 1078, pp. 8-15 https://doi.org/10.1016/j.aca.2019.06.038 

 

Anzardi, M.B., Arancibia, J.A., Olivieri, A.C.Interpretation of matrix chromatographic-spectral data modeling with parallel factor analysis 2 and multivariate curve resolution (2019) Journal of Chromatography A, 1604, art. no. 460502, https://doi.org/10.1016/j.chroma.2019.460502 

 

Chiappini, F.A., Alcaraz, M.R., Goicoechea, H.C., Olivieri, A.C. A graphical user interface as a new tool for scattering correction in fluorescence data (2019) Chemometrics and Intelligent Laboratory Systems, 193, art. no. 103810 https://doi.org/10.1016/j.chemolab.2019.07.009 

 

Tomat, D., Soazo, M., Verdini, R., Casabonne, C., Aquili, V., Balagué, C., Quiberoni, A. Evaluation of an WPC edible film added with a cocktail of six lytic phages against foodborne pathogens such as enteropathogenic and Shigatoxigenic Escherichia coli (2019) LWT, 113, art. no. 108316 https://doi.org/10.1016/j.lwt.2019.108316 

 

Della-Felice, F., Sarotti, A.M., Krische, M.J., Pilli, R.A.Total Synthesis and Structural Validation of Phosdiecin A via Asymmetric Alcohol-Mediated Carbonyl Reductive Coupling (2019) Journal of the American Chemical Society, 141 (35), pp. 13778-13782 https://doi.org/10.1021/jacs.9b07512 

 

Pagani, A.P., Ibañez, G.A. Pesticide residues in fruits and vegetables: High-order calibration based on spectrofluorimetric/pH data (2019) Microchemical Journal, 149, art. no. 104042 https://doi.org/10.1016/j.microc.2019.104042 

 

Heredia, D.A., Martínez, S.R., Durantini, A.M., Pérez, M.E., Mangione, M.I., Durantini, J.E., Gervaldo, M.A., Otero, L.A., Durantini, E.N. Antimicrobial Photodynamic Polymeric Films Bearing Biscarbazol Triphenylamine End-Capped Dendrimeric Zn(II) Porphyrin (2019) ACS Applied Materials and Interfaces, 11 (31), pp. 27574-27587 https://doi.org/10.1021/acsami.9b09119 

 

Kaufman, T.S. Selected aspects of the chemical and biological profile of triclabendazole, a widely used benzimidazole fasciolicidal agent (2019) Advances in Chemistry Research. Volume 55, pp. 83-134 http://hdl.handle.net/11336/117655

 

 

Calvo, N.L., Sreekumar, S., Svetaz, L.A., Lamas, M.C., Moerschbacher, B.M., Leonardi, D. Design and characterization of chitosan nanoformulations for the delivery of antifungal agents (2019) International Journal of Molecular Sciences, 20 (15), art. no. 3686, https://doi.org/10.3390/ijms20153686

 

Medrán, N.S., Dezotti, F., Pellegrinet, S.C. Remarkable Reactivity of Boron-Substituted Furans in the Diels-Alder Reactions with Maleic Anhydride (2019) Organic Letters, 21 (13), pp. 5068-5072 https://doi.org/10.1021/acs.orglett.9b01662 

 

Grimblat, N., Gavín, J.A., Hernández Daranas, A., Sarotti, A.M. Combining the Power of J Coupling and DP4 Analysis on Stereochemical Assignments: The J-DP4 Methods (2019) Organic Letters, 21 (11), pp. 4003-4007 https://doi.org/10.1021/acs.orglett.9b0119

 

Salazar-Rojas, D., Intilangelo, A., Vignaduzzo, S.E., Maggio, R.M. Development and validation of a green method for dissolution monitoring of pharmaceutical combinations. Meloxican and pridinol (2019) Journal of Pharmaceutical and Biomedical Analysis, 170, pp. 228-233. https://doi.org/10.1016/j.jpba.2019.03.038 

 

Antonio, M., Calvo, N.L., Maggio, R.M. Chemometric study of the excipients’ influence on polymorphic-behavior. Mefenamic acid as case of study (2019) Journal of Pharmaceutical and Biomedical Analysis, 170, pp. 8-15 https://doi.org/10.1016/j.jpba.2019.03.021 

 

Simonetti, S.O., Pellegrinet, S.C. Asymmetric Organocatalytic C-C Bond Forming Reactions with Organoboron Compounds: A Mechanistic Survey (2019) European Journal of Organic Chemistry, 2019 (19), pp. 2956-2970 https://doi.org/10.1002/ejoc.201900029 

 

Brites, N.P., Dilelio, M.C., Martins, G.M., Carmo, G.D., Morel, A.F., Kaufman, T.S., Silveira, C.C. Synthesis and Antifungal Activity of 4- and 6-(1H-Pyrrol-1-yl) Coumarins, and their Thiocyanato Derivatives (2019) ChemistrySelect, 4 (19), pp. 5398-5406. https://doi.org/10.1002/slct.201900842

 

Carabajal, M.D., Arancibia, J.A., Escandar, G.M. Excitation-emission fluorescence-kinetic third-order/four-way data: Determination of bisphenol A and nonylphenol in food-contact plastics (2019) Talanta, 197, pp. 348-355 https://doi.org/10.1016/j.talanta.2019.01.045

 

Seremeta, K.P., Arrúa, E.C., Okulik, N.B., Salomon, C.J. Development and characterization of benznidazole nano- and microparticles: A new tool for pediatric treatment of Chagas disease? (2019) Colloids and Surfaces B: Biointerfaces, 177, pp. 169-177 https://doi.org/10.1016/j.colsurfb.2019.01.039

 

Patriarca, M., Daier, V., Camí, G., Pellegri, N., Rivière, E., Hureau, C., Signorella, S. Biomimetic Cu, Zn and Cu2 complexes inserted in mesoporous silica as catalysts for superoxide dismutation (2019) Microporous and Mesoporous Materials, 279, pp. 133-141 https://doi.org/10.1016/j.micromeso.2018.12.027

 

Jiménez-Carvelo, A.M., Cruz, C.M., Olivieri, A.C., González-Casado, A., Cuadros-Rodríguez, L. Classification of olive oils according to their cultivars based on second-order data using LC-DAD (2019) Talanta, 195, pp. 69-76 https://doi.org/10.1016/j.talanta.2018.11.033

 

Mangione, M.I., Cappellari, M.V., Fungo, F., Spanevello, R.A. Novel Turtle-Shape Dendrimers Based on a Pyrene Core (2019) ChemistrySelect, 4 (11), pp. 3113-3117 https://doi.org/10.1002/slct.201900191

 

Riveira, M.J., Martiren, N.L., Mischne, M.P. Domino Self-Sensitized Photooxygenation of Conjugated Dienones for the Synthesis of 1,2,4-Trioxanes (2019) Journal of Organic Chemistry, 84 (6), pp. 3671-3677 https://doi.org/10.1021/acs.joc.8b03279

 

Martins, G.M., do Carmo, G., Morel, A.F., Kaufman, T.S., Silveira, C.C. A Convenient and Atom-Economic One-Pot Selenium-Chloride-Mediated Synthesis of 2-Arylselenopheno[2,3-b]indoles and Their Antifungal Activity (2019) Asian Journal of Organic Chemistry, 8 (3), pp. 369-375 https://doi.org/10.1002/ajoc.201900028

 

Braga, L.R., Pérez, L.M., Soazo, M.D.V., Machado, F. Evaluation of the antimicrobial, antioxidant and physicochemical properties of Poly(Vinyl chloride) films containing quercetin and silver nanoparticles (2019) LWT, 101, pp. 491-498 https://doi.org/10.1016/j.lwt.2018.11.082

 

Escandar, G.M., Olivieri, A.C. Multi-way chromatographic calibration—A review (2019) Journal of Chromatography A, 1587, pp. 2-13. https://doi.org/10.1016/j.chroma.2019.01.012

 

Zanardi, M.M., Sortino, M.A., Sarotti, A.M. On the effect of intramolecular H-bonding in the configurational assessment of polyhydroxylated compounds with computational methods. The hyacinthacines case, (2019) Carbohydrate Research, 474, pp. 72-79. https://doi.org/10.1016/j.carres.2019.01.011

 

García, A., Priotti, J., Codina, A.V., Vasconi, M.D., Quiroga, A.D., Hinrichsen, L.I., Leonardi, D., Lamas, M.C. Synthesis and characterization of a new cyclodextrin derivative with improved properties to design oral dosage forms (2019) Drug Delivery and Translational Research, 9 (1), pp. 273-283 https://doi.org/10.1007/s13346-018-0591-8

 

Calvo, N.L., Svetaz, L.A., Alvarez, V.A., Quiroga, A.D., Lamas, M.C., Leonardi, D. Chitosan-hydroxypropyl methylcellulose tioconazole films: A promising alternative dosage form for the treatment of vaginal candidiasis (2019) International Journal of Pharmaceutics, 556, pp. 181-191 https://doi.org/10.1016/j.ijpharm.2018.12.011

 

Vargas, D.F., Larghi, E.L., Kaufman, T.S.The 6π-azaelectrocyclization of azatrienes. Synthetic applications in natural products, bioactive heterocycles, and related fields (2019) Natural Product Reports, 36 (2), pp. 354-401 https://doi.org/10.1039/c8np00014j

 

Calvo, N.L., Alvarez, V.A., Lamas, M.C., Leonardi, D. New approaches to identification and characterization of tioconazole in raw material and in pharmaceutical dosage forms (2019) Journal of Pharmaceutical Analysis, 9 (1), pp. 40-48. https://doi.org/10.1016/j.jpha.2018.11.006

 

Pérez Mora, B.E., Bellú, S.E., Mangiameli, M.F., García, S.I., González, J.C. Optimization of continuous arsenic biosorption present in natural contaminated groundwater (2019) Journal of Chemical Technology and Biotechnology, 94 (2), pp. 547-555. https://doi.org/10.1002/jctb.5801

 

Jiménez-Carvelo, A.M., Lozano, V.A., Olivieri, A.C. Comparative chemometric analysis of fluorescence and near infrared spectroscopies for authenticity confirmation and geographical origin of Argentinean extra virgin olive oils (2019) Food Control, 96, pp. 22-28. https://doi.org/10.1016/j.foodcont.2018.08.024

 

Piccirilli, G.N., Soazo, M., Pérez, L.M., Delorenzi, N.J., Verdini, R.A. Effect of storage conditions on the physicochemical characteristics of edible films based on whey protein concentrate and liquid smoke (2019) Food Hydrocolloids, 87, pp. 221-228 https://doi.org/10.1016/j.foodhyd.2018.08.015

 

Cankařová, N., La Venia, A., Krajčovičová, S., Krchňák, V. Configuration-Dependent Medium-Sized Ring Formation: Chiral Molecular Framework with Three-Dimensional Architecture (2019) Journal of Organic Chemistry, 84 (2), pp. 636-644 https://doi.org/10.1021/acs.joc.8b02465

 

Pagani, A.P., Ibañez, G.A. Analytical approach for the simultaneous determination of quinolones in edible animal products. Modeling pH–modulated fluorescence excitation–emission matrices four–way arrays (2019) Talanta, 192, pp. 52-60 https://doi.org/10.1016/j.talanta.2018.09.015

 

Li, C., Sarotti, A.M., Wu, X., Yang, B., Turkson, J., Chen, Y., Liu, Q., Cao, S. An unusual benzoisoquinoline-9-one derivative and other related compounds with antiproliferative activity from Hawaiian endophytic fungus Peyronellaea sp. FT431 (2019) Molecules, 24 (1), art. no. 196 https://doi.org/10.3390/molecules24010196

 

Palopoli, C., Ferreyra, J., Conte-Daban, A., Richezzi, M., Foi, A., Doctorovich, F., Anxolabéhère-Mallart, E., Hureau, C., Signorella, S.R. Insights into Second-Sphere Effects on Redox Potentials, Spectroscopic Properties, and Superoxide Dismutase Activity of Manganese Complexes with Schiff-Base Ligands (2019) ACS Omega, 4 (1), pp. 48-57 https://doi.org/10.1021/acsomega.8b03018

 

Mostardeiro, V.B., Dilelio, M.C., Kaufman, T.S., Silveira, C.C. Efficient synthesis of 4-sulfanylcoumarins from 3-bromo-coumarins: Via a highly selective DABCO-mediated one-pot thia-Michael addition/elimination process (2019) RSC Advances, 10 (1), pp. 482-491 https://doi.org/10.1039/c9ra09545d

 

Aguilar, A.A.A., Ledesma, G.N., Tirloni, B., Kaufman, T.S., Larghi, E.L. Convergent First Total Synthesis of Melovinone: A Densely Substituted 3-Methoxy-4-quinolone Isolated from Melochia tomentosa L (2019) Synthesis (Germany), 51 (22), pp. 4253-4262 https://doi.org/10.1055/s-0039-1690164

 

Vargas, D.F., Larghi, E.L., Kaufman, T.S. First total synthesis of ampullosine, a unique isoquinoline alkaloid isolated from Sepedonium ampullosporum, and of the related permethylampullosine (2019) RSC Advances, 9 (57), pp. 33096-33106 https://doi.org/10.1039/c9ra06839b

 

Fonzo, S., Vargas, D.F., Kaufman, T.S. A Ruthenium-Catalyzed C-H Activation Strategy as an Efficient Shortcut in the Total Synthesis of 6,8-Dimethoxy-1,3-dimethylÂ-isoquinoline (2019) Synthesis (Germany), 51 (20), pp. 3908-3914 https://doi.org/10.1055/s-0037-1610720

 

de Luco, J.F., Prez, G., Cravero, B.H., de Mendoza, D., Labadie, G.R. Synthesis of a deuterated standard for the quantification of 2-arachidonoylglycerol in caenorhabditis elegans (2019) Journal of Visualized Experiments, 2019 (151), art. no. e59882 https://doi.org/10.3791/59882

 

Porta, E.O.J., Bofill Verdaguer, I., Perez, C., Banchio, C., Ferreira De Azevedo, M., Katzin, A.M., Labadie, G.R. Repositioning Salirasib as a new antimalarial agent (2019) MedChemComm, 10 (9), pp. 1599-1605 https://doi.org/10.1039/c9md00298g

 

Mazarío, J., Parreño Romero, M., Concepción, P., Chávez-Sifontes, M., Spanevello, R.A., Comba, M.B., Suárez, A.G., Domine, M.E. Tuning zirconia-supported metal catalysts for selective one-step hydrogenation of levoglucosenone (2019) Green Chemistry, 21 (17), pp. 4769-4785 https://doi.org/10.1039/c9gc01857c

 

Stortz, C.A., Sarotti, A.M. Exhaustive exploration of the conformational landscape of mono- and disubstituted five-membered rings by DFT and MP2 calculations (2019) RSC Advances, 9 (42), pp. 24134-24145 https://doi.org/10.1039/c9ra03524a

 

Dilelio, M.C., Brites, N.P., Vieira, L.A., Iglesias, B.A., Kaufman, T.S., Silveira, C.C. Synthesis and Photophysical Properties of 1,4-Dihydro-2 H,5H-chromeno[4,3-D][1,3]oxazin-5-ones, and Derivatives Containing Tethered 1,2,3-Triazoles, from 4-Aminocoumarins (2019) Synthesis (Germany), 51 (15), pp. 2965-2976 https://doi.org/10.1055/s-0037-1612428

 

Méndez, M.V., Simonetti, S.O., Kaufman, T.S., Bracca, A.B.J. A concise Friedländer/Buchwald-Hartwig approach to the total synthesis of quindoline, a bioactive natural indoloquinoline alkaloid, and toward the unnatural 10-methylquindoline (2019) New Journal of Chemistry, 43 (27), pp. 10803-10813 https://doi.org/10.1039/c9nj01961h

 

Vargas, D.F., Larghi, E.L., Kaufman, T.S. Concise Synthesis of the ABC-Ring System of the Azafluoranthene, Tropoisoquinoline and Proaporphine Alkaloids: An Olefin Hydroacylation/Pomeranz-Fritsch Cyclization Approach (2019) Synthesis (Germany), 51 (9), pp. 2030-2038 https://doi.org/10.1055/s-0037-1611711

 

Della-Felice, F., De Assis, F.F., Sarotti, A.M., Pilli, R.A. Palladium-Catalyzed Formation of Substituted Tetrahydropyrans: Mechanistic Insights and Structural Revision of Natural Products (2019) Synthesis (Germany), 51 (7), pp. 1545-1560 https://doi.org/10.1055/s-0037-1611708

 

Medran, N.S., La-Venia, A., Testero, S.A. Metal-mediated synthesis of pyrrolines (2019) RSC Advances, 9 (12), pp. 6804-6844 https://doi.org/10.1039/c8ra10247c

 

Cortés, I., Borini Etichetti, C.M., Girardini, J.E., Kaufman, T.S., Bracca, A.B.J. Total Synthesis and Cytotoxic Activity of 6,8-Dimethoxy-1,3-dimethylisoquinoline Isolated from Ancistrocladus tectorius: A 6π-Azaelectrocyclization Approach (2019) Synthesis (Germany), 51 (2), pp. 433-440 https://doi.org/10.1055/s-0037-1610276

 

Jäger, S.N., Porta, E.O.J., Labadie, G.R. Convenient synthesis of the immunogenic glycolipid BbGL1 (2019) Steroids, 141, pp. 41-45 https://doi.org/10.1016/j.steroids.2018.11.012

2018

Comba, M.B., Mangione, M.I., Suárez, A.G., Sarotti, A.M., Spanevello, R.A. A Domino Epoxide Ring-Opening Xanthate Migration Reaction: An Alternative Entry to Thiosugars (2018) European Journal of Organic Chemistry, 2018 (48), pp. 6848-6856 https://doi.org/10.1002/ejoc.201801432

 

Real, D., Hoffmann, S., Leonardi, D., Salomon, C., Goycoolea, F.M. Chitosan-based nanodelivery systems applied to the development of novel triclabendazole formulations (2018) PLoS ONE, 13 (12), art. no. e0207625 https://doi.org/10.1371/journal.pone.0207625

 

Sabatini, M., Comba, S., Altabe, S., Recio-Balsells, A.I., Labadie, G.R., Takano, E., Gramajo, H., Arabolaza, A. Biochemical characterization of the minimal domains of an iterative eukaryotic polyketide synthase (2018) FEBS Journal, 285 (23), pp. 4494-4511 https://doi.org/10.1111/febs.14675

 

Gera, J., Szögi, T., Bozsó, Z., Fülöp, L., Barrera, E.E., Rodriguez, A.M., Méndez, L., Delpiccolo, C.M.L., Mata, E.G., Cioffi, F., Broersen, K., Paragi, G., Enriz, R.D. Searching for improved mimetic peptides inhibitors preventing conformational transition of amyloid-β 42 monomer (2018) Bioorganic Chemistry, 81, pp. 211-221. https://doi.org/10.1016/j.bioorg.2018.08.018

 

Pisano, P.L., Espino, M., Fernández, M.D.L.Á., Silva, M.F., Olivieri, A.C. Structural analysis of natural deep eutectic solvents. Theoretical and experimental study (2018) Microchemical Journal, 143, pp. 252-258. https://doi.org/10.1016/j.microc.2018.08.016

 

Galles, C., Prez, G.M., Penkov, S., Boland, S., Porta, E.O.J., Altabe, S.G., Labadie, G.R., Schmidt, U., Knölker, H.-J., Kurzchalia, T.V., De Mendoza, D. Endocannabinoids in Caenorhabditis elegans are essential for the mobilization of cholesterol from internal reserves (2018) Scientific Reports, 8 (1), art. no. 6398. https://doi.org/10.1038/s41598-018-24925-8

 

Pellegrino Vidal, R.B., Olivieri, A.C., Ibanez, G.A., Escandar, G.M. Online Third-Order Liquid Chromatographic Data with Native and Photoinduced Fluorescence Detection for the Quantitation of Organic Pollutants in Environmental Water (2018) ACS Omega, 3 (11), pp. 15771-15779. https://doi.org/10.1021/acsomega.8b02439

 

Marsili, L.A., Pergomet, J.L., Gandon, V., Riveira, M.J. Iodine-Catalyzed Iso-Nazarov Cyclization of Conjugated Dienals for the Synthesis of 2-Cyclopentenones (2018) Organic Letters, 20 (22), pp. 7298-7303. https://doi.org/10.1021/acs.orglett.8b03229

 

Vargas, D.F., Larghi, E.L., Kaufman, T.S. Synthesis of Polysubstituted 3-Methylisoquinolines through the 6π-Electron Cyclization/Elimination of 1-Azatrienes derived from 1,1-Dimethylhydrazine (2018) European Journal of Organic Chemistry, 2018 (40), pp. 5605-5614. https://doi.org/10.1002/ejoc.201801076

 

Priotti, J., Baglioni, M.V., García, A., Rico, M.J., Leonardi, D., Lamas, M.C., Menacho Márquez, M. Repositioning of Anti-parasitic Drugs in Cyclodextrin Inclusion Complexes for Treatment of Triple-Negative Breast Cancer (2018) AAPS PharmSciTech, 19 (8), pp. 3734-3741. https://doi.org/10.1208/s12249-018-1169-y

 

Tejada, G., Lamas, M.C., Sortino, M., Alvarez, V.A., Leonardi, D. Composite Microparticles Based on Natural Mucoadhesive Polymers with Promising Structural Properties to Protect and Improve the Antifungal Activity of Miconazole Nitrate (2018) AAPS PharmSciTech, 19 (8), pp. 3712-3722. https://doi.org/10.1208/s12249-018-1175-0

 

Mazivila, S.J., Olivieri, A.C. Chemometrics coupled to vibrational spectroscopy and spectroscopic imaging for the analysis of solid-phase pharmaceutical products: A brief review on non-destructive analytical methods (2018) TrAC – Trends in Analytical Chemistry, 108, pp. 74-87. https://doi.org/10.1016/j.trac.2018.08.013

 

Carabajal, M.D., Arancibia, J.A., Escandar, G.M. Multivariate curve resolution strategy for non-quadrilinear type 4 third-order/four way liquid chromatography–excitation-emission fluorescence matrix data (2018) Talanta, 189, pp. 509-516. https://doi.org/10.1016/j.talanta.2018.07.017

 

Priotti, J., García, A., Leonardi, D., Ferreira, M.J., Lamas, M.C., Nunes, T.G. Succinyl-β-cyclodextrin: Influence of the substitution degree on albendazole inclusion complexes probed by NMR (2018) Materials Science and Engineering C, 92, pp. 694-702. https://doi.org/10.1016/j.msec.2018.07.013

 

Lombardi, J.M., Bortolato, S.A. Functional data analysis, a new approach to aligning three-way liquid chromatographic with fluorescence detection data (2018) Microchemical Journal, 142, pp. 219-228. https://doi.org/10.1016/j.microc.2018.06.041

 

Batistelli, M., Martínez Bilesio, A.R., García-Reiriz, A.G. Development of a fast and inexpensive method for detecting the main sediment sources in a river basin (2018) Microchemical Journal, 142, pp. 208-218. https://doi.org/10.1016/j.microc.2018.06.040

 

Morri, M., Castellano, P., Leonardi, D., Vignaduzzo, S. Correction to: First Development, Optimization, and Stability Control of a Pediatric Oral Atenolol Formulation (AAPS PharmSciTech, (2018), 19, 4, (1781-1788), 10.1208/s12249-018-0992-5) (2018) AAPS PharmSciTech, 19 (8), p. 3907. https://doi.org/10.1208/s12249-018-1014-3

 

Prada Gori, D.N., Permingeat Squizatto, C., Cornier, P.G., Delpiccolo, C.M.L. Design of a Selective Ring-Closing Enyne Metathesis-Reduction for the Generation of Different Synthetic Scaffolds (2018) Journal of Organic Chemistry, 83 (20), pp. 12798-12805. https://doi.org/10.1021/acs.joc.8b01511

 

Zanardi, M.M., Biglione, F.A., Sortino, M.A., Sarotti, A.M. General Quantum-Based NMR Method for the Assignment of Absolute Configuration by Single or Double Derivatization: Scope and Limitations (2018) Journal of Organic Chemistry, 83 (19), pp. 11839-11849. https://doi.org/10.1021/acs.joc.8b01749

 

Chen, N., Lee, N., Bortolato, S.A., Martino, D.M. Experimental studies and mathematical modeling of the curing reaction of bioinspired copolymers (2018) Green Chemistry Letters and Reviews, 11 (4), pp. 387-398. https://doi.org/10.1080/17518253.2018.1516809

 

Silva, L.D., Lima, N.F., Arrua, E.C., Salomon, C.J., Vinaud, M.C. In vivo treatment of experimental neurocysticercosis with praziquantel nanosuspensions—a metabolic approach (2018) Drug Delivery and Translational Research, 8 (5), pp. 1265-1273. https://doi.org/10.1007/s13346-018-0576-7

 

Ramírez, C.L., Mangione, M.I., Bertolotti, S.G., Arbeloa, E.M., Parise, A.R. A photophysical and spectroelectrochemical study on N-phenyl-carbazoles and their oxidized species (2018) Journal of Photochemistry and Photobiology A: Chemistry, 365, pp. 199-207. https://doi.org/10.1016/j.jphotochem.2018.07.039

 

Cai, Y.-S., Sarotti, A.M., Zhou, T.-L., Huang, R., Qiu, G., Tian, C., Miao, Z.-H., Mándi, A., Kurtán, T., Cao, S., Yang, S.-P. Flabellipparicine, a Flabelliformide-Apparicine-Type Bisindole Alkaloid from Tabernaemontana divaricata (2018) Journal of Natural Products, 81 (9), pp. 1976-1983. https://doi.org/10.1021/acs.jnatprod.8b00191

 

Torres Manno, M., Zuljan, F., Alarcón, S., Esteban, L., Blancato, V., Espariz, M., Magni, C. Genetic and phenotypic features defining industrial relevant Lactococcus lactis, L. cremoris and L. lactis biovar. diacetylactis strains (2018) Journal of Biotechnology, 282, pp. 25-31. https://doi.org/10.1016/j.jbiotec.2018.06.345

 

Riveira, M.J., Diez, C.M., Mischne, M.P., Mata, E.G. -Cycloaddition Reactions Using Immobilized Alkynes. A Proof of Concept for an Integral Use of the Outcoming Products in Solid-Phase Synthetic Methodologies (2018) Journal of Organic Chemistry, 83 (17), pp. 10001-10014. https://doi.org/10.1021/acs.joc.8b01378

 

Tejada, G., Lamas, M.C., Svetaz, L., Salomón, C.J., Alvarez, V.A., Leonardi, D. Effect of drug incorporation technique and polymer combination on the performance of biopolymeric antifungal buccal films (2018) International Journal of Pharmaceutics, 548 (1), pp. 431-442. https://doi.org/10.1016/j.ijpharm.2018.07.023

 

Calvo, N.L., Balzaretti, N.M., Antonio, M., Kaufman, T.S., Maggio, R.M. Chemometrics-assisted study of the interconversion between the crystalline forms of nimodipine (2018) Journal of Pharmaceutical and Biomedical Analysis, 158, pp. 461-470. https://doi.org/10.1016/j.jpba.2018.06.019

 

Estébanez, S., Lorente, C., Kaufman, T.S., Larghi, E.L., Thomas, A.H., Serrano, M.P. Photophysical and Photochemical Properties of 3-methylpterin as a New and More Stable Pterin-type Photosensitizer (2018) Photochemistry and Photobiology, 94 (5), pp. 881-889. https://doi.org/10.1111/php.12931

 

Franceschelli, J.J., Belardinelli, J.M., Tong, P., Loftus, B., Recio-Balsells, A., Labadié, G.R., Gordon, S.V., Morbidoni, H.R. A katG S315T or an ahpC promoter mutation mediate Mycobacterium tuberculosis resistance to 2-thiophen carboxylic acid hydrazide, an inhibitor resembling the anti-tubercular drugs Isoniazid and Ethionamide (2018) Tuberculosis, 112, pp. 69-78. https://doi.org/10.1016/j.tube.2018.08.001

 

Salazar, M.O., Pisano, P.L., González Sierra, M., Furlan, R.L.E. NMR and multivariate data analysis to assess traceability of argentine citrus (2018) Microchemical Journal, 141, pp. 264-270. https://doi.org/10.1016/j.microc.2018.05.037

 

Ledesma, G.N., Anxolabéhère-Mallart, E., Sabater, L., Hureau, C., Signorella, S.R. Functional modeling of the MnCAT active site with a dimanganese(III) complex of an unsymmetrical polydentate N 3 O 3 ligand (2018) Journal of Inorganic Biochemistry, 186, pp. 10-16. https://doi.org/10.1016/j.jinorgbio.2018.04.023

 

Ghaffari, M., Olivieri, A.C., Abdollahi, H. Strategy to Obtain Accurate Analytical Solutions in Second-Order Multivariate Calibration with Curve Resolution Methods (2018) Analytical Chemistry, 90 (16), pp. 9725-9733. https://doi.org/10.1021/acs.analchem.8b00336

 

Arroyo Aguilar, A.A., Bolívar Avila, S.J., Kaufman, T.S., Larghi, E.L. Total Synthesis of Waltherione F, a Nonrutaceous 3-Methoxy-4-quinolone, Isolated from Waltheria indica L. F. (2018) Organic Letters, 20 (16), pp. 5058-5061. https://doi.org/10.1021/acs.orglett.8b02221

 

Salvatori, P.E., Sánchez, G., Lombardi, A., Nicocia, E., Bortolato, S.A., Boschetti, C.E. Optimization of properties in a rubber compound containing a ternary polymer blend using response surface methodology (2018) Journal of Applied Polymer Science, 135 (30), art. no. 46548. https://doi.org/10.1002/app.46548

 

Riveira, M.J., Marcarino, M.O., La-Venia, A. Multicomponent Domino Synthesis of Cyclopenta[ b]furan-2-ones (2018) Organic Letters, 20 (13), pp. 4000-4004. https://doi.org/10.1021/acs.orglett.8b01567

 

Allegrini, F., Braga, J.W.B., Moreira, A.C.O., Olivieri, A.C. Error Covariance Penalized Regression: A novel multivariate model combining penalized regression with multivariate error structure (2018) Analytica Chimica Acta, 1011, pp. 20-27. https://doi.org/10.1016/j.aca.2018.02.002

 

Signorella, S., Palopoli, C., Ledesma, G. Rationally designed mimics of antioxidant manganoenzymes: Role of structural features in the quest for catalysts with catalase and superoxide dismutase activity (2018) Coordination Chemistry Reviews, 365, pp. 75-102. https://doi.org/10.1016/j.ccr.2018.03.005

 

Pellegrino Vidal, R.B., Olivieri, A.C., Tauler, R. Quantifying the Prediction Error in Analytical Multivariate Curve Resolution Studies of Multicomponent Systems (2018) Analytical Chemistry, 90 (11), pp. 7040-7047. https://doi.org/10.1021/acs.analchem.8b01431

 

García, V.S., Peverengo, L., Peretti, L.E., González, V.D.G., Gugliotta, L.M., Dalla Fontana, M.L., Marcipar, I.S., Lagier, C.M. An improved approach to estimate the avidity index of immunoglobulins: Evaluation of the method using IgG anti-Toxoplasma gondii (2018) Journal of Immunological Methods, 457, pp. 78-81. https://doi.org/10.1016/j.jim.2018.03.008

 

Cortés, I., Kaufman, T.S., Bracca, A.B.J. A convenient and eco-friendly cerium(III) chloride-catalysed synthesis of methoxime derivatives of aromatic aldehydes and ketones (2018) Royal Society Open Science, 5 (5), art. no. 180279, https://doi.org/10.1098/rsos.180279

 

Demicheli, V., Moreno, D.M., Radi, R. Human Mn-superoxide dismutase inactivation by peroxynitrite: A paradigm of metal-catalyzed tyrosine nitration: In vitro and in vivo (2018) Metallomics, 10 (5), pp. 679-695. https://doi.org/10.1039/c7mt00348j

 

Morri, M., Castellano, P., Leonardi, D., Vignaduzzo, S. First Development, Optimization, and Stability Control of a Pediatric Oral Atenolol Formulation (2018) AAPS PharmSciTech, 19 (4), pp. 1781-1788. https://doi.org/10.1208/s12249-018-0992-5

 

Della-Felice, F., Pilli, R.A., Sarotti, A.M. Computer-Guided total synthesis of natural products. Recent examples and future perspectives (2018) Journal of the Brazilian Chemical Society, 29 (5), pp. 1041-1075. https://doi.org/10.21577/0103-5053.20180027

 

Solís, V., Palopoli, C., Daier, V., Rivière, E., Collin, F., Moreno, D.M., Hureau, C., Signorella, S. Tuning the Mn II 2 /Mn III 2 redox cycle of a phenoxo-bridged diMn catalase mimic with terminal carboxylate donors (2018) Journal of Inorganic Biochemistry, 182, pp. 29-36. https://doi.org/10.1016/j.jinorgbio.2018.01.013

 

Heredia, D.A., Durantini, A.M., Sarotti, A.M., Gsponer, N.S., Ferreyra, D.D., Bertolotti, S.G., Milanesio, M.E., Durantini, E.N. Proton-Dependent Switching of a Novel Amino Chlorin Derivative as a Fluorescent Probe and Photosensitizer for Acidic Media (2018) Chemistry – A European Journal, 24 (22), pp. 5950-5961. https://doi.org/10.1002/chem.201800060

 

Tsai, Y.-H., Borini Etichetti, C.M., Di Benedetto, C., Girardini, J.E., Martins, F.T., Spanevello, R.A., Suárez, A.G., Sarotti, A.M. Synthesis of triazole derivatives of levoglucosenone as promising anticancer agents: Effective exploration of the chemical space through retro-za-michael//aza-michael isomerizations (2018) Journal of Organic Chemistry, 83 (7), pp. 3516-3528. https://doi.org/10.1021/acs.joc.7b03141

 

Méndez, M.V., Bracca, A.B.J., Kaufman, T.S. Isolation, Synthesis, and Biological Activity of Quindoline, a Valuable Indoloquinoline Natural Product and Useful Key Intermediate (2018) Synthesis (Germany), 50 (7), art. no. ss-2017-z0830-sr, pp. 1417-1429. https://doi.org/10.1055/s-0036-1591947

 

Orlandi, S., Priotti, J., Diogo, H.P., Leonardi, D., Salomon, C.J., Nunes, T.G. Structural Elucidation of Poloxamer 237 and Poloxamer 237/Praziquantel Solid Dispersions: Impact of Poly(Vinylpyrrolidone) over Drug Recrystallization and Dissolution (2018) AAPS PharmSciTech, 19 (3), pp. 1274-1286. https://doi.org/10.1208/s12249-017-0946-3

 

González, L.J., Stival, C., Puzzolo, J.L., Moreno, D.M., Vila, A.J. Shaping substrate selectivity in a broad-spectrum metallo-β-lactamase (2018) Antimicrobial Agents and Chemotherapy, 62 (4), art. no. e02079-17. https://doi.org/10.1128/AAC.02079-17

 

Pedroso, M., Gehn, A.Z., Stivanin, M.L., Larghi, E.L., Burrow, R.A., Resende, J.A.L.C., Da Silva, U.F., Mostardeiro, M.A., Dalcol, I.I., Morel, A.F. Absolute configuration of clemateol (2018) Journal of the Brazilian Chemical Society, 29 (4), pp. 881-887. https://doi.org/10.21577/0103-5053.20170189

 

Priotti, J., Leonardi, D., Pico, G., Lamas, M.C. Application of Fluorescence Emission for Characterization of Albendazole and Ricobendazole Micellar Systems: Elucidation of the Molecular Mechanism of Drug Solubilization Process (2018) AAPS PharmSciTech, 19 (3), pp. 1152-1159. https://doi.org/10.1208/s12249-017-0927-6

 

Pellegrino Vidal, R.B., Allegrini, F., Olivieri, A.C. The effect of constraints on the analytical figures of merit achieved by extended multivariate curve resolution-alternating least-squares (2018) Analytica Chimica Acta, 1003, pp. 10-15. https://doi.org/10.1016/j.aca.2017.12.008

 

Martins, G.M., Back, D.F., Kaufman, T.S., Silveira, C.C. SeCl2-Mediated Approach Toward Indole-Containing Polysubstituted Selenophenes (2018) Journal of Organic Chemistry, 83 (6), pp. 3252-3264. https://doi.org/10.1021/acs.joc.8b00166

 

Riveira, M.J., Sarotti, A.M. NMR and experimental reinvestigation of the condensation reaction between γ-methylene-α,β-unsaturated aldehydes and propargyl aldehydes (2018) Organic and Biomolecular Chemistry, 16 (9), pp. 1442-1447. https://doi.org/10.1039/c7ob03110f

 

Orrillo, A.G., La-Venia, A., Escalante, A.M., Furlan, R.L.E. Rewiring Chemical Networks Based on Dynamic Dithioacetal and Disulfide Bonds (2018) Chemistry – A European Journal, 24 (13), pp. 3141-3146. https://doi.org/10.1002/chem.201705654

 

Aleixandre-Tudo, J.L., Nieuwoudt, H., Olivieri, A., Aleixandre, J.L., du Toit, W. Phenolic profiling of grapes, fermenting samples and wines using UV-Visible spectroscopy with chemometrics (2018) Food Control, 85, pp. 11-22. https://doi.org/10.1016/j.foodcont.2017.09.014

 

Pergomet, J.L., Di Liberto, M.G., Derita, M.G., Bracca, A.B.J., Kaufman, T.S. Activity of the pterophyllins 2 and 4 against postharvest fruit pathogenic fungi. Comparison with a synthetic analog and related intermediates (2018) Fitoterapia, 125, pp. 98-105. https://doi.org/10.1016/j.fitote.2017.12.021

 

Mazivila, S.J., Bortolato, S.A., Olivieri, A.C. MVC3_GUI: A MATLAB graphical user interface for third-order multivariate calibration. An upgrade including new multi-way models (2018) Chemometrics and Intelligent Laboratory Systems, 173, pp. 21-29. https://doi.org/10.1016/j.chemolab.2017.12.012

 

Mangione, M.I., Spanevello, R.A., Minudri, D., Cavallo, P., Otero, L., Fungo, F. Electrochemical films deposition and electro-optical properties of bis-carbazol-triphenylamine end-caped dendrimeric polymers (2018) Electrochimica Acta, 263, pp. 585-595. https://doi.org/10.1016/j.electacta.2017.12.137

 

Comba, M.B., Tsai, Y.-H., Sarotti, A.M., Mangione, M.I., Suárez, A.G., Spanevello, R.A. Levoglucosenone and Its New Applications: Valorization of Cellulose Residues (2018) European Journal of Organic Chemistry, 2018 (5), pp. 590-604. https://doi.org/10.1002/ejoc.201701227

 

Antonio, M., Maggio, R.M. Assessment of mefenamic acid polymorphs in commercial tablets using chemometric coupled to MIR and NIR spectroscopies. Prediction of dissolution performance (2018) Journal of Pharmaceutical and Biomedical Analysis, 149, pp. 603-611. https://doi.org/10.1016/j.jpba.2017.11.053

 

Granato, D., Santos, J.S., Escher, G.B., Ferreira, B.L., Maggio, R.M. Use of principal component analysis (PCA) and hierarchical cluster analysis (HCA) for multivariate association between bioactive compounds and functional properties in foods: A critical perspective (2018) Trends in Food Science and Technology, 72, pp. 83-90. https://doi.org/10.1016/j.tifs.2017.12.006

 

Tomat, D., Balagué, C., Aquili, V., Verdini, R., Quiberoni, A. Resistance of phages lytic to pathogenic Escherichia coli to sanitisers used by the food industry and in home settings (2018) International Journal of Food Science and Technology, 53 (2), pp. 533-540. https://doi.org/10.1111/ijfs.13626

 

Mortera, P., Zuljan, F.A., Magni, C., Bortolato, S.A., Alarcón, S.H. Multivariate analysis of organic acids in fermented food from reversed-phase high-performance liquid chromatography data (2018) Talanta, 178, pp. 15-23. https://doi.org/10.1016/j.talanta.2017.09.005

 

Bertoni, F.A., González, J.C., García, S.I., Sala, L.F., Bellú, S.E. Application of chitosan in removal of molybdate ions from contaminated water and groundwater (2018) Carbohydrate Polymers, 180, pp. 55-62. https://doi.org/10.1016/j.carbpol.2017.10.027

 

Calvo, N.L., Maggio, R.M., Kaufman, T.S. Characterization of pharmaceutically relevant materials at the solid state employing chemometrics methods (2018) Journal of Pharmaceutical and Biomedical Analysis, 147, pp. 538-564. https://doi.org/10.1016/j.jpba.2017.06.017

 

Calvo, N.L., Maggio, R.M., Kaufman, T.S. Chemometrics-assisted solid-state characterization of pharmaceutically relevant materials. Polymorphic substances (2018) Journal of Pharmaceutical and Biomedical Analysis, 147, pp. 518-537.https://doi.org/10.1016/j.jpba.2017.06.018

 

Li, C., Sarotti, A.M., Yoshida, W., Cao, S. Two new polyketides from Hawaiian endophytic fungus Pestalotiopsis sp. FT172 (2018) Tetrahedron Letters, 59 (1), pp. 42-45. https://doi.org/10.1016/j.tetlet.2017.11.045

 

Cappellari, M.V., Mangione, M.I., Spanevello, R.A., Marzari, G., Morales, G.M., Fungo, F. Design and synthesis of efficient electrogenerated chemiluminescent emitters derived from pyrene (2018) Journal of the Electrochemical Society, 165 (14), pp. G163-G170. https://doi.org/10.1149/2.0881814jes

 

Navarro, M.V., Cabezón, M.A., Damiani, P.C. Simultaneous determination of pesticides in fruits by using second-order fluorescence data resolved by unfolded partial least-squares coupled to residual bilinearization (2018) Journal of Chemistry, 2018, art. no. 3217465. https://doi.org/10.1155/2018/3217465

 

Spanevello, R.A., Suárez, A.G. Education and outreach: Key elements to promote the responsible and peaceful uses of chemistry (2018) ACS Symposium Series, 1288, pp. 69-81. https://doi.org/10.1021/bk-2018-1288.ch004

 

Pisano, P.L., Pellegrinet, S.C. Alkylhalovinylboranes: a new class of Diels-Alder dienophiles (2018) RSC Advances, 8 (59), pp. 33864-33871. https://doi.org/10.1039/C8RA07089J

 

Puzzolo, J.L., Drusin, S.I., Daier, V.A., Signorella, S., Moreno, D.M. Using theoretical calculations to predict the redox potential of mononuclear manganese complexes (2018) New Journal of Chemistry, 42 (18), pp. 14827-14831. https://doi.org/10.1039/c8nj03254h

 

Mangiameli, M.F., Bellú, S., Pérez Mora, B., Sala, L., Mamana, N. Quinic acid and hypervalent chromium: A spectroscopic and kinetic study (2018) RSC Advances, 8 (51), pp. 29356-29367. https://doi.org/10.1039/c8ra03809k

 

Da Silva, C.C., Valdo, A.K., Do Nascimento Neto, J.A., Ribeiro, L., Sarotti, A.M., Martins, F.T. Why lamivudine assembles into double-stranded helices in crystals: Salt heterosynthon: Versus base-pairing homosynthon (2018) CrystEngComm, 20 (22), pp. 3049-3057. https://doi.org/10.1039/c8ce00100f

 

Méndez, L., Poeylaut-Palena, A.A., Mata, E.G. Molecular diversity by olefin cross-metathesis on solid support. Generation of libraries of biologically promising β-lactam derivatives (2018) Molecules, 23 (5), art. no. 1193. https://doi.org/10.3390/molecules23051193

 

Blank, V., Bellizzi, Y., Zotta, E., Cornier, P.G., Delpiccolo, C.M.L., Boggián, D.B., Mata, E.G., Roguin, L.P. A novel penicillin derivative induces antitumor effect in melanoma cells (2018) Anti-Cancer Drugs, 29 (5), pp. 416-428. https://doi.org/10.1097/CAD.0000000000000611

 

La-Venia, A., Mischne, M.P., Mata, E.G. Gold-catalyzed addition of β-ketoesters to alkenes: Influence of electronic and steric effects in the reaction outcome (2018) Molecules, 23 (3), art. no. 629. https://doi.org/10.3390/molecules23030629

 

Sarotti, A.M. Structural revision of two unusual rhamnofolane diterpenes, curcusones I and J, by means of DFT calculations of NMR shifts and coupling constants (2018) Organic and Biomolecular Chemistry, 16 (6), pp. 944-950. https://doi.org/10.1039/c7ob02916k

 

Panozzo-Zénere, E.A., Porta, E.O.J., Arrizabalaga, G., Fargnoli, L., Khan, S.I., Tekwani, B.L., Labadie, G.R. A minimalistic approach to develop new anti-apicomplexa polyamines analogs (2018) European Journal of Medicinal Chemistry, 143, pp. 866-880. https://doi.org/10.1016/j.ejmech.2017.11.069

 

Lombardi, J., Pellegrino, J.M., Soazo, M., Corrêa, A.P.F., Brandelli, A., Risso, P., Boeris, V. Mineral fortification modifies physical and microstructural characteristics of milk gels coagulated by a bacterial enzymatic pool (2018) Colloids and Surfaces B: Biointerfaces, 161, pp. 296-301. https://doi.org/10.1016/j.colsurfb.2017.10.043

2017

Pontoriero, A., Mosconi, N., Monti, L., Bellú, S., Williams, P.A.M., Raimondi, M., Lima, B., Feresin, G.E., Nerli, B., Rizzotto, M. Synthesis, characterization and biological studies of a cobalt(III) complex of sulfathiazole (2017) Chemico-Biological Interactions, 278, pp. 152-161. https://doi.org/10.1016/j.cbi.2017.10.004

 

Giordano, P.C., Goicoechea, H.C., Olivieri, A.C. SRO_ANN: An integrated MatLab toolbox for multiple surface response optimization using radial basis functions (2017) Chemometrics and Intelligent Laboratory Systems, 171, pp. 198-206. https://doi.org/10.1016/j.chemolab.2017.11.004

 

Mancilla Canales, M.A., Leguto, A.J., Riquelme, B.D., León, P.P.D., Bortolato, S.A., Korol, A.M. Hurst exponent: A Brownian approach to characterize the nonlinear behavior of red blood cells deformability (2017) Physica A: Statistical Mechanics and its Applications, 488, pp. 1-7. https://doi.org/10.1016/j.physa.2017.06.009

 

Carabajal, M.D., Arancibia, J.A., Escandar, G.M. On-line generation of third-order liquid chromatography–excitation-emission fluorescence matrix data. Quantitation of heavy-polycyclic aromatic hydrocarbons (2017) Journal of Chromatography A, 1527, pp. 61-69. https://doi.org/10.1016/j.chroma.2017.10.057

 

Santos Souza, H.F., Real, D., Leonardi, D., Rocha, S.C., Alonso, V., Serra, E., Silber, A.M., Salomon, C.J. Development and in vitro/in vivo evaluation of a novel benznidazole liquid dosage form using a quality-by-design approach (2017) Tropical Medicine and International Health, 22 (12), pp. 1514-1522. https://doi.org/10.1111/tmi.12980

 

Lisa, M.-N., Palacios, A.R., Aitha, M., González, M.M., Moreno, D.M., Crowder, M.W., Bonomo, R.A., Spencer, J., Tierney, D.L., Llarrull, L.I., Vila, A.J. A general reaction mechanism for carbapenem hydrolysis by mononuclear and binuclear metallo-β-lactamases (2017) Nature Communications, 8 (1), art. no. 538. https://doi.org/10.1038/s41467-017-00601-9

 

Li, C.-S., Sarotti, A.M., Huang, P., Dang, U.T., Hurdle, J.G., Kondratyuk, T.P., Pezzuto, J.M., Turkson, J., Cao, S. NF-κB inhibitors, unique γ-pyranol-γ-lactams with sulfide and sulfoxide moieties from Hawaiian plant Lycopodiella cernua derived fungus Paraphaeosphaeria neglecta FT462 (2017) Scientific Reports, 7 (1), art. no. 10424. https://doi.org/10.1038/s41598-017-10537-1

 

Ceccoli, R.D., Bianchi, D.A., Fink, M.J., Mihovilovic, M.D., Rial, D.V. Cloning and characterization of the Type I Baeyer–Villiger monooxygenase from Leptospira biflexa (2017) AMB Express, 7 (1), art. no. 87. https://doi.org/10.1186/s13568-017-0390-5

 

Batista Braga, J.W., Allegrini, F., Olivieri, A.C. Maximum likelihood unfolded principal component regression with residual bilinearization (MLU-PCR/RBL) for second-order multivariate calibration (2017) Chemometrics and Intelligent Laboratory Systems, 170, pp. 51-57. https://doi.org/10.1016/j.chemolab.2017.09.016

 

Sayé, M., Fargnoli, L., Reigada, C., Labadie, G.R., Pereira, C.A. Evaluation of proline analogs as trypanocidal agents through the inhibition of a Trypanosoma cruzi proline transporter (2017) Biochimica et Biophysica Acta – General Subjects, 1861 (11), pp. 2913-2921. https://doi.org/10.1016/j.bbagen.2017.08.015

 

Galante, M., Pavón, Y., Lazzaroni, S., Soazo, M., Costa, S., Boeris, V., Risso, P., Rozycki, S. Effect of cholesterol-reduced and zinc fortification treatments on physicochemical, functional, textural, microstructural and sensory properties of soft cheese (2017) International Journal of Dairy Technology, 70 (4), pp. 533-541. https://doi.org/10.1111/1471-0307.12361

 

Giri, G.F., Viarengo, G., Furlán, R.L.E., Suárez, A.G., Eleonora, G.V., Spanevello, R.A. Soybean hulls, an alternative source of bioactive compounds: Combining pyrolysis with bioguided fractionation (2017) Industrial Crops and Products, 105, pp. 113-123. https://doi.org/10.1016/j.indcrop.2017.05.005

 

Tejada, G., Piccirilli, G.N., Sortino, M., Salomón, C.J., Lamas, M.C., Leonardi, D. Formulation and in-vitro efficacy of antifungal mucoadhesive polymeric matrices for the delivery of miconazole nitrate (2017) Materials Science and Engineering C, 79, pp. 140-150. https://doi.org/10.1016/j.msec.2017.05.034

 

Della-Felice, F., Sarotti, A.M., Pilli, R.A. Catalytic Asymmetric Synthesis and Stereochemical Revision of (+)-Cryptoconcatone H (2017) Journal of Organic Chemistry, 82 (17), pp. 9191-9197. https://doi.org/10.1021/acs.joc.7b01378

 

Martins, F.T., De Freitas Oliveira, B.G., Sarotti, A.M., De Fátima, A. Winged-cone conformation in hexa-p-tert-butylcalix[6]arene driven by the unusually strong guest encapsulation (2017) ACS Omega, 2 (8), pp. 5315-5323. https://doi.org/10.1021/acsomega.7b00900

 

Escandar, G.M., Olivieri, A.C. A road map for multi-way calibration models (2017) Analyst, 142 (16), pp. 2862-2873. https://doi.org/10.1039/c7an00822h

 

Castillo, M.V., Pergomet, J.L., Carnavale, G.A., Davies, L., Zinczuk, J., Brandán, S.A. FTIR, FTRaman, UV–Visible and NMR spectroscopic studies on 3,3′,4,4′-tetrachloroazoxybenzene, an azoxybenzene derivative with toxic effects (2017) Journal of Molecular Structure, 1142, pp. 18-27. https://doi.org/10.1016/j.molstruc.2017.04.043

 

Li, C., Sarotti, A.M., Yang, B., Turkson, J., Cao, S. A New N-methoxypyridone from the Co-Cultivation of Hawaiian Endophytic Fungi Camporesia sambuci FT1061 and Epicoccum sorghinum FT1062 (2017) Molecules (Basel, Switzerland), 22 (7).  https://doi.org/10.3390/molecules22071166

 

Bianchi, P., Varela, R.F., Bianchi, D.A., Kemppainen, M., Iribarren, A.M., Lewkowicz, E. Selection of microbial biocatalysts for the reduction of cyclic and heterocyclic ketones (2017) Process Biochemistry, 58, pp. 137-144. https://doi.org/10.1016/j.procbio.2017.04.039

 

Boeris, V., Arancibia, J.A., Olivieri, A.C. Multivariate curve resolution applied to kinetic-spectroscopic data matrices: Dye determination in foods by means of enzymatic oxidation (2017) Talanta, 169, pp. 189-194. https://doi.org/10.1016/j.talanta.2017.03.079

 

Privitera, M.L., Lozano, V.A. Development of a second-order standard addition fluorescence method for the direct determination of riboflavin in human urine samples without previous clean up and separation steps (2017) Microchemical Journal, 133, pp. 60-66. https://doi.org/10.1016/j.microc.2017.02.033

 

Li, C., Sarotti, A.M., Turkson, J., Cao, S. Verbenanone, an octahydro-5H-chromen-5-one from a Hawaiian-plant associated fungus FT431 (2017) Tetrahedron Letters, 58 (23), pp. 2290-2293. https://doi.org/10.1016/j.tetlet.2017.04.096

 

Vallejos, M.M., Pellegrinet, S.C. Theoretical Study of the BF3-Promoted Rearrangement of Oxiranyl N-Methyliminodiacetic Acid Boronates (2017) Journal of Organic Chemistry, 82 (11), pp. 5917-5925. https://doi.org/10.1021/acs.joc.7b01096

 

Vignaduzzo, S.E., Operto, M.A., Castellano, P.M. Development of a dissolution test for fenbendazole-praziquantel capsules using UV-PLS method (2017) Journal of the Brazilian Chemical Society, 28 (6), pp. 1030-1037. https://doi.org/10.21577/0103-5053.20160258

 

Cieślak, A., Wauthoz, N., Nieto Orellana, A., Lautram, N., Béjaud, J., Hureaux, J., Lafleur, M., Benoit, J.-P., Salomon, C.J., Bastiat, G. Stealth nanocarriers based sterosomes using PEG post-insertion process (2017) European Journal of Pharmaceutics and Biopharmaceutics, 115, pp. 31-38. https://doi.org/10.1016/j.ejpb.2017.02.008

 

Carnevale, B., Blanes, P., Sala, L.F., Bellú, S.E. Removal of molybdate anions from contaminated waters by brown algae biomass in batch and continuous processes (2017) Journal of Chemical Technology and Biotechnology, 92 (6), pp. 1298-1305. https://doi.org/10.1002/jctb.5124

 

Delpiccolo, C.M.L., Martinez-Amezaga, M., Mata, E.G. Recent approaches toward the generation of molecular diversity based on β-lactam structures (2017) Beta-Lactams: Novel Synthetic Pathways and Applications, pp. 129-162. ttps://doi.org/10.1007/978-3-319-55621-5_5

 

Soberón, J.R., Sgariglia, M.A., Pastoriza, A.C., Soruco, E.M., Jäger, S.N., Labadie, G.R., Sampietro, D.A., Vattuone, M.A. Antifungal activity and cytotoxicity of extracts and triterpenoid saponins obtained from the aerial parts of Anagallis arvensis L. (2017) Journal of Ethnopharmacology, 203, pp. 233-240. https://doi.org/10.1016/j.jep.2017.03.056

 

Priotti, J., Codina, A.V., Leonardi, D., Vasconi, M.D., Hinrichsen, L.I., Lamas, M.C. Albendazole Microcrystal Formulations Based on Chitosan and Cellulose Derivatives: Physicochemical Characterization and In Vitro Parasiticidal Activity in Trichinella spiralis Adult Worms (2017) AAPS PharmSciTech, 18 (4), pp. 947-956. https://doi.org/10.1208/s12249-016-0659-z

 

Salomon, C., Goycoolea, F.M., Moerschbacher, B. Recent Trends in the Development of Chitosan-Based Drug Delivery Systems (2017) AAPS PharmSciTech, 18 (4), pp. 933-935. https://doi.org/10.1208/s12249-017-0764-7

 

Priotti, J., Codina, A.V., Leonardi, D., Vasconi, M.D., Hinrichsen, L.I., Lamas, M.C. Albendazole Microcrystal Formulations Based on Chitosan and Cellulose Derivatives: Physicochemical Characterization and In Vitro Parasiticidal Activity in Trichinella spiralis Adult Worms (2017) AAPS PharmSciTech, 18 (4), pp. 947-956. https://doi.org/10.1208/s12249-016-0659-z

 

Tejada, G., Barrera, M.G., Piccirilli, G.N., Sortino, M., Frattini, A., Salomón, C.J., Lamas, M.C., Leonardi, D. Development and Evaluation of Buccal Films Based on Chitosan for the Potential Treatment of Oral Candidiasis (2017) AAPS PharmSciTech, 18 (4), pp. 936-946. https://doi.org/10.1208/s12249-017-0720-6

 

Müller, G.L., Tuttobene, M., Altilio, M., Amezaga, M.M., Nguyen, M., Cribb, P., Cybulski, L.E., Ramírez, M.S., Altabe, S., Mussi, M.A. Light modulates metabolic pathways and other novel physiological traits in the human pathogen Acinetobacter baumannii (2017) Journal of Bacteriology, 199 (10), art. no. e00011-17. https://doi.org/10.1128/JB.00011-17

 

Pagani, A.P., Ibañez, G.A. Four-way calibration applied to the processing of pH-modulated fluorescence excitation-emission matrices. Analysis of fluoroquinolones in the presence of significant spectral overlapping (2017) Microchemical Journal, 132, pp. 211-218. https://doi.org/10.1016/j.microc.2017.01.028

 

Riveira, M.J., Mata, E.G. Cross-Metathesis on Immobilized Substrates – Application to the Generation of Synthetically and Biologically Relevant Structures (2017) European Journal of Organic Chemistry, 2017 (13), pp. 1675-1693. https://doi.org/10.1002/ejoc.201601487

 

Martinez-Amezaga, M., Delpiccolo, C.M.L., Méndez, L., Dragutan, I., Dragutan, V., Mata, E.G. Unprecedented multifunctionality of grubbs and hoveyda–grubbs catalysts: Competitive isomerization, hydrogenation, silylation and metathesis occurring in solution and on solid phase (2017) Catalysts, 7 (4), art. no. 111. https://doi.org/10.3390/catal7040111

 

Báez, G.D., Piccirilli, G.N., Ballerini, G.A., Frattini, A., Busti, P.A., Verdini, R.A., Delorenzi, N.J. Physicochemical Characterization of a Heat Treated Calcium Alginate Dry Film Prepared with Chicken Stock (2017) Journal of Food Science, 82 (4), pp. 945-951. https://doi.org/10.1111/1750-3841.13658

 

Carabajal, M.D., Arancibia, J.A., Escandar, G.M. Excitation-emission fluorescence-kinetic data obtained by Fenton degradation. Determination of heavy-polycyclic aromatic hydrocarbons by four-way parallel factor analysis (2017) Talanta, 165, pp. 52-63. https://doi.org/10.1016/j.talanta.2016.12.030

 

Pellegrino Vidal, R.B., Ibañez, G.A., Escandar, G.M. Advantages of Data Fusion: First Multivariate Curve Resolution Analysis of Fused Liquid Chromatographic Second-Order Data with Dual Diode Array-Fluorescent Detection (2017) Analytical Chemistry, 89 (5), pp. 3029-3035. https://doi.org/10.1021/acs.analchem.6b04720

 

Senf, D., Ruprecht, C., de Kruijff, G.H.M., Simonetti, S.O., Schuhmacher, F., Seeberger, P.H., Pfrengle, F. Active Site Mapping of Xylan-Deconstructing Enzymes with Arabinoxylan Oligosaccharides Produced by Automated Glycan Assembly (2017) Chemistry – A European Journal, 23 (13), pp. 3197-3205. https://doi.org/10.1002/chem.201605902

 

Costa, J.G., Peretti, L.E., García, V.S., Peverengo, L., González, V.D.G., Gugliotta, L.M., Dalla Fontana, M.L., Lagier, C.M., Marcipar, I.S. P35 and P22 Toxoplasma gondii antigens abbreviate regions to diagnose acquired toxoplasmosis during pregnancy: Toward single-sample assays (2017) Clinical Chemistry and Laboratory Medicine, 55 (4), pp. 595-604. https://doi.org/10.1515/cclm-2016-0331

 

Olivieri, A.C., Tauler, R. The effect of data matrix augmentation and constraints in extended multivariate curve resolution–alternating least squares (2017) Journal of Chemometrics, 31 (3), art. no. e2875. https://doi.org/10.1002/cem.2875

 

Zanardi, M.M., Suárez, A.G., Sarotti, A.M. Determination of the Relative Configuration of Terminal and Spiroepoxides by Computational Methods. Advantages of the Inclusion of Unscaled Data (2017) Journal of Organic Chemistry, 82 (4), pp. 1873-1879. https://doi.org/10.1021/acs.joc.6b02129

 

Allegrini, F., Olivieri, A.C. Recent advances in analytical figures of merit: Heteroscedasticity strikes back (2017) Analytical Methods, 9 (5), pp. 739-743. https://doi.org/10.1039/c6ay02916g

 

Suárez, A.G. Education and engagement: Key elements to achieve and maintain a world free of chemical weapons (2017) Pure and Applied Chemistry, 89 (2), pp. 197-204. https://doi.org/10.1515/pac-2016-0901

 

Palopoli, C., Gómez, G., Foi, A., Doctorovich, F., Mallet-Ladeira, S., Hureau, C., Signorella, S. Dimerization, redox properties and antioxidant activity of two manganese(III) complexes of difluoro- and dichloro-substituted Schiff-base ligands (2017) Journal of Inorganic Biochemistry, 167, pp. 49-59. https://doi.org/10.1016/j.jinorgbio.2016.11.019

 

Padilha, G., Iglesias, B.A., Back, D.F., Kaufman, T.S., Silveira, C.C. Synthesis of Chromeno[4,3-b]pyrrol-4(1H)-ones, from β-Nitroalkenes and 4-Phenylaminocoumarins, under Solvent–free Conditions (2017) ChemistrySelect, 2 (3), pp. 1297-1304. https://doi.org/10.1002/slct.201700114

 

Ledesma, G., Signorella, S., Back, D., Schulz Lang, E. Crystal structure of cis-1-phenyl-8-(pyridin-2-ylmethyl)dibenzo[1,2-c:2,1-h]-2,14-dioxa-8-aza-1-borabicyclo[4.4.0]deca-3,8-diene (2017) Acta Crystallographica Section E: Crystallographic Communications, 73, pp. 1917-1920. https://doi.org/10.1107/S2056989017016553

 

Riveira, M.J., Marsili, L.A., Mischne, M.P. The iso-Nazarov reaction (2017) Organic and Biomolecular Chemistry, 15 (44), pp. 9255-9274. https://doi.org/10.1039/c7ob02220d

 

Do Nascimento Neto, J.A., Da Silva, C.C., Ribeiro, L., Vasconcelos, G.A., Gontijo Vaz, B., Ferreira, V.S., Queiroz Júnior, L.H.K., Maia, L.J.Q., Sarotti, A.M., Martins, F.T. Probing the competition between acetate and 2,2′-bipyridine ligands to bind to d-block group 12 metals (2017) New Journal of Chemistry, 41 (21), pp. 12843-12853. https://doi.org/10.1039/c7nj02393f

 

Valdo, A.K.S.M., Sarotti, A.M., Martins, F.T. Synthon trends according to acid strength and geometry in salts of N-heterocyclic bases (2017) CrystEngComm, 19 (40), pp. 5960-5965. https://doi.org/10.1039/c7ce01490b

 

Mangione, M.I., Spanevello, R.A., Anzardi, M.B. Efficient and straightforward click synthesis of structurally related dendritic triazoles (2017) RSC Advances, 7 (75), pp. 47681-47688. https://doi.org/10.1039/c7ra09558a

 

Porta, E.O.J., Vallejos, M.M., Bracca, A.B.J., Labadie, G.R. Experimental and theoretical studies of the [3,3]-sigmatropic rearrangement of prenyl azides (2017) RSC Advances, 7 (75), pp. 47527-47538. https://doi.org/10.1039/c7ra09759j

 

Cai, Y.-S., Sarotti, A.M., Gündisch, D., Kondratyuk, T.P., Pezzuto, J.M., Turkson, J., Cao, S. Heliotropiumides A and B, new phenolamides with N-carbamoyl putrescine moiety from Heliotropium foertherianum collected in Hawaii and their biological activities (2017) Bioorganic and Medicinal Chemistry Letters, 27 (20), pp. 4630-4634. https://doi.org/10.1016/j.bmcl.2017.09.021

 

Pergomet, J.L., Bracca, A.B.J., Kaufman, T.S. Total syntheses of gerberinol i and the pterophyllins 2 and 4 using the Casnati-Skattebøl reaction under different conditions (2017) Organic and Biomolecular Chemistry, 15 (33), pp. 7040-7049. https://doi.org/10.1039/c7ob01471f

 

Martinez-Amezaga, M., Delpiccolo, C.M.L., Mata, E.G. Immobilized boronic acid for Suzuki-Miyaura coupling: Application to the generation of pharmacologically relevant molecules (2017) RSC Advances, 7 (56), pp. 34994-35003. https://doi.org/10.1039/c7ra06662g

 

Porta, E.O.J., Jäger, S.N., Nocito, I., Lepesheva, G.I., Serra, E.C., Tekwani, B.L., Labadie, G.R. Antitrypanosomal and antileishmanial activity of prenyl-1,2,3-triazoles (2017) MedChemComm, 8 (5), pp. 1015-1021. https://doi.org/10.1039/c7md00008a

 

Méndez, M.V., Heredia, D.A., Larghi, E.L., Bracca, A.B.J., Kaufman, T.S. Efficient total synthesis of neocryptolepine and synthetic access to 6-methylquinindoline from a common intermediate (2017) RSC Advances, 7 (45), pp. 28298-28307. https://doi.org/10.1039/c7ra05349e

 

Martins, F.T., Maia, L.J.Q., Da Silva Neto, L., Da Silva, C.M., Sarotti, A.M., De Fátima, Â. Solvatomorphs of 25,26,27,28-tetrahydroxycalix[4]arene and 5,11,17,23-tetramino-25,26,27,28-tetrabutoxycalix[4]arene: quenching photoluminescence through switching the guest (2017) CrystEngComm, 19 (13), pp. 1792-1800. https://doi.org/10.1039/c6ce02649d

 

Huang, P., Li, C., Sarotti, A.M., Turkson, J., Cao, S. Sphaerialactonam, a γ-lactam–isochromanone from the Hawaiian endophytic fungus Paraphaeosphaeria sp. FT462 (2017) Tetrahedron Letters, 58 (13), pp. 1330-1333. https://doi.org/10.1016/j.tetlet.2017.02.052

 

Padilha, G., Birmann, P.T., Domingues, M., Kaufman, T.S., Savegnago, L., Silveira, C.C. Convenient Michael addition/β-elimination approach to the synthesis of 4-benzyl- and 4-aryl-selenyl coumarins using diselenides as selenium sources (2017) Tetrahedron Letters, 58 (10), pp. 985-990. https://doi.org/10.1016/j.tetlet.2017.01.084

 

Pergomet, J.L., Larghi, E.L., Kaufman, T.S., Bracca, A.B.J. First total synthesis of the only known 2-isopropyliden-2: H -benzofuran-3-one isolated from V. luetzelburgii (2017) RSC Advances, 7 (9), pp. 5242-5250. https://doi.org/10.1039/c6ra28587b

 

Valdo, A.K.S.M., Da Silva, C.C., Maia, L.J.Q., Sarotti, A.M., Martins, F.T. Experimental and theoretical second harmonic generation and photoluminescence from the pseudo-centrosymmetric dihydrochloride salt dihydrate of trans-1,2-bis(4-pyridyl)ethene (2017) CrystEngComm, 19 (2), pp. 346-354. https://doi.org/10.1039/c6ce02229d

 

Gerosa, G.G., Grimblat, N., Spanevello, R.A., Suárez, A.G., Sarotti, A.M. Mechanistic insight into the acid-catalyzed isomerization of biomass-derived polysubstituted pyrrolidines: an experimental and DFT study (2017) Organic and Biomolecular Chemistry, 15 (2), pp. 426-434.

https://doi.org/10.1039/c6ob02457b

 

Arias, D.G., Herrera, F.E., Garay, A.S., Rodrigues, D., Forastieri, P.S., Luna, L.E., Bürgi, M.D.L.M., Prieto, C., Iglesias, A.A., Cravero, R.M., Guerrero, S.A. Rational design of nitrofuran derivatives: Synthesis and valuation as inhibitors of Trypanosoma cruzi trypanothione reductase (2017) European Journal of Medicinal Chemistry, 125, pp. 1088-1097. https://doi.org/10.1016/j.ejmech.2016.10.055

 

Ghiano, D.G., de la Iglesia, A., Liu, N., Tonge, P.J., Morbidoni, H.R., Labadie, G.R. Antitubercular activity of 1,2,3-triazolyl fatty acid derivatives (2017) European Journal of Medicinal Chemistry, 125, pp. 842-852. https://doi.org/10.1016/j.ejmech.2016.09.086

2016

Grimblat, N., Kaufman, T.S., Sarotti, A.M. Computational Chemistry Driven Solution to Rubriflordilactone B (2016) Organic Letters, 18 (24), pp. 6420-6423. https://doi.org/10.1021/acs.orglett.6b03318

 

Simonetti, S.O., Larghi, E.L., Kaufman, T.S. The 3,4-dioxygenated 5-hydroxy-4-aryl-quinolin-2(1: H)-one alkaloids. Results of 20 years of research, uncovering a new family of natural products (2016) Natural Product Reports, 33 (12), pp. 1425-1446. https://doi.org/10.1039/c6np00064a

 

Pérez, R.L., Escandar, G.M. Experimental and chemometric strategies for the development of Green Analytical Chemistry (GAC) spectroscopic methods for the determination of organic pollutants in natural waters (2016) Sustainable Chemistry and Pharmacy, 4, pp. 1-12.

https://doi.org/10.1016/j.scp.2016.06.003

 

Allegrini, F., Olivieri, A.C. Multi-way figures of merit in the presence of heteroscedastic and correlated instrumental noise: Unfolded partial least-squares with residual multi-linearization (2016) Chemometrics and Intelligent Laboratory Systems, 158, pp. 200-209. https://doi.org/10.1016/j.chemolab.2016.09.001

 

Monago-Maraña, O., Pérez, R.L., Escandar, G.M., Muñoz De La Peña, A., Galeano-Díaz, T. Combination of Liquid Chromatography with Multivariate Curve Resolution-Alternating Least-Squares (MCR-ALS) in the Quantitation of Polycyclic Aromatic Hydrocarbons Present in Paprika Samples (2016) Journal of Agricultural and Food Chemistry, 64 (43), pp. 8254-8262. https://doi.org/10.1021/acs.jafc.6b03852

 

Zuljan, F.A., Mortera, P., Alarcón, S.H., Blancato, V.S., Espariz, M., Magni, C. Lactic acid bacteria decarboxylation reactions in cheese (2016) International Dairy Journal, 62, pp. 53-62. https://doi.org/10.1016/j.idairyj.2016.07.007

 

Giulidori, C., Mosconi, N., Toplikar, B., Vega, M., Williams, P., Svetaz, L., Raimondi, M., Rizzotto, M. Heteroleptic complexes of antifungal drugs with the silver ion (2016) Journal of Physical Organic Chemistry, 29 (11), pp. 656-664. https://doi.org/10.1002/poc.3603

 

Ficarra, F.A., Santecchia, I., Lagorio, S.H., Alarcón, S., Magni, C., Espariz, M. Genome mining of lipolytic exoenzymes from Bacillus safensis S9 and Pseudomonas alcaliphila ED1 isolated from a dairy wastewater lagoon (2016) Archives of Microbiology, 198 (9), pp. 893-904. https://doi.org/10.1007/s00203-016-1250-4

 

Lozano, V.A., Escandar, G.M. Simultaneous determination of urea herbicides in water and soil samples based on second-order photoinduced fluorescence data (2016) Analytical Methods, 8 (40), pp. 7396-7404. https://doi.org/10.1039/c6ay02136k

 

Husbands, J.L., Suárez, A.G. The Hague Ethical Guidelines: applying the norms of the practice of chemistry to support the Chemical Weapons Convention (2016) Toxicological and Environmental Chemistry, 98 (9), pp. 1110-1114.https://doi.org/10.1080/02772248.2016.1172074

 

Sussmann, R.A.C., de Moraes, M.M., Cebrián-Torrejón, G., Porta, E.O., Doménech-Carbó, A., Yamaguchi, L.F., Katzin, A.M., Kato, M.J. Stabilization and detection of hydrophylloquinone as di-O-methyl derivative (2016) Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, 1033-1034, pp. 368-371. https://doi.org/10.1016/j.jchromb.2016.09.011

 

Padró, J.M., Osorio-Grisales, J., Arancibia, J.A., Olivieri, A.C., Castells, C.B. Enantiomeric analysis of overlapped chromatographic profiles in the presence of interferences. Determination of ibuprofen in a pharmaceutical formulation containing homatropine (2016) Journal of Chromatography A, 1467, pp. 255-260. https://doi.org/10.1016/j.chroma.2016.05.094

 

Karak, M., Acosta, J.A.M., Barbosa, L.C.A., Sarotti, A.M., Da Silva, C.C., Boukouvalas, J., Martins, F.T. Substituent-Modulated Conformation and Supramolecular Assembly of Tetronamides (2016) Crystal Growth and Design, 16 (10), pp. 5798-5810. https://doi.org/10.1021/acs.cgd.6b00881

 

Daier, V.A., Rivière, E., Mallet-Ladeira, S., Moreno, D.M., Hureau, C., Signorella, S.R. Synthesis, characterization and activity of imidazolate-bridged and Schiff-base dinuclear complexes as models of Cu,Zn-SOD. A comparative study (2016) Journal of Inorganic Biochemistry, 163, pp. 162-175. https://doi.org/10.1016/j.jinorgbio.2016.07.008

 

Morán-Barrio, J., Lisa, M.-N., Larrieux, N., Drusin, S.I., Viale, A.M., Moreno, D.M., Buschiazzo, A., Vila, A.J. Crystal structure of the metallo-β-lactamase GOB in the periplasmic dizinc form reveals an unusual metal site (2016) Antimicrobial Agents and Chemotherapy, 60 (10), pp. 6013-6022. https://doi.org/10.1128/AAC.01067-16

 

Vidal, R.B.P., Ibañez, G.A., Escandar, G.M. A green method for the quantification of plastics-derived endocrine disruptors in beverages by chemometrics-assisted liquid chromatography with simultaneous diode array and fluorescent detection (2016) Talanta, 159, pp. 336-343. https://doi.org/10.1016/j.talanta.2016.06.049

 

Soazo, M., Pérez, L.M., Piccirilli, G.N., Delorenzi, N.J., Verdini, R.A. Antimicrobial and physicochemical characterization of whey protein concentrate edible films incorporated with liquid smoke (2016) LWT, 72, pp. 285-291. https://doi.org/10.1016/j.lwt.2016.04.027

 

Costa, E.D., Priotti, J., Orlandi, S., Leonardi, D., Lamas, M.C., Nunes, T.G., Diogo, H.P., Salomon, C.J., Ferreira, M.J. Unexpected solvent impact in the crystallinity of praziquantel/poly(vinylpyrrolidone) formulations. A solubility, DSC and solid-state NMR study (2016) International Journal of Pharmaceutics, 511 (2), pp. 983-993. https://doi.org/10.1016/j.ijpharm.2016.08.009

 

Calvo, N.L., Arias, J.M., Altabef, A.B., Maggio, R.M., Kaufman, T.S. Determination of the main solid-state form of albendazole in bulk drug, employing Raman spectroscopy coupled to multivariate analysis (2016) Journal of Pharmaceutical and Biomedical Analysis, 129, pp. 190-197. https://doi.org/10.1016/j.jpba.2016.07.013

 

Riveira, M.J., La-Venia, A., Mischne, M.P. Pericyclic Cascade toward Isochromenes: Application to the Synthesis of Alkaloid Benzosimuline (2016) Journal of Organic Chemistry, 81 (17), pp. 7977-7983. https://doi.org/10.1021/acs.joc.6b01278

 

Van Doorslaer, S., Beirinckx, Q., Nys, K., Mangiameli, M.F., Cuypers, B., Callens, F., Vrielinck, H., González, J.C. EPR and DFT analysis of biologically relevant chromium(V) complexes with D-glucitol and D-glucose (2016) Journal of Inorganic Biochemistry, 162, pp. 216-226. https://doi.org/10.1016/j.jinorgbio.2016.07.012

 

Silva, L.D., Arrúa, E.C., Pereira, D.A., Fraga, C.M., da Costa, T.L., Hemphill, A., Salomon, C.J., Vinaud, M.C. Elucidating the influence of praziquantel nanosuspensions on the in vivo metabolism of Taenia crassiceps cysticerci (2016) Acta Tropica, 161, pp. 100-105. https://doi.org/10.1016/j.actatropica.2016.06.002

 

Carabajal, M.D., Arancibia, J.A., Escandar, G.M. A green-analytical chemistry method for agrochemical-residue analysis in vegetables (2016) Microchemical Journal, 128, pp. 34-41. https://doi.org/10.1016/j.microc.2016.03.006

 

Fragoso, W.D., Olivieri, A.C. Chemometric modeling of kinetic-fluorescent third-order data for thiamine determination in multivitamin complexes (2016) Microchemical Journal, 128, pp. 42-46. https://doi.org/10.1016/j.microc.2016.04.006

 

Allegrini, F., Fernández Pierna, J.A., Fragoso, W.D., Olivieri, A.C., Baeten, V., Dardenne, P. Regression models based on new local strategies for near infrared spectroscopic data (2016) Analytica Chimica Acta, 933, pp. 50-58. https://doi.org/10.1016/j.aca.2016.07.006

 

Fragoso, W., Allegrini, F., Olivieri, A.C. A new and consistent parameter for measuring the quality of multivariate analytical methods: Generalized analytical sensitivity (2016) Analytica Chimica Acta, 933, pp. 43-49. https://doi.org/10.1016/j.aca.2016.06.022

 

Grimblat, N., Sarotti, A.M. Computational Chemistry to the Rescue: Modern Toolboxes for the Assignment of Complex Molecules by GIAO NMR Calculations (2016) Chemistry – A European Journal, 22 (35), pp. 12246-12261. https://doi.org/10.1002/chem.201601150

 

La-Venia, A., Medran, N.S., Krchňák, V., Testero, S.A. Synthesis of a Small Library of Imidazolidin-2-ones using Gold Catalysis on Solid Phase (2016) ACS Combinatorial Science, 18 (8), pp. 482-489. https://doi.org/10.1021/acscombsci.6b00062

 

Fortes, M.P., Da Silva, P.B.N., Da Silva, T.G., Kaufman, T.S., Militão, G.C.G., Silveira, C.C. Synthesis and preliminary evaluation of 3-thiocyanato-1H-indoles as potential anticancer agents (2016) European Journal of Medicinal Chemistry, 118, pp. 21-26. https://doi.org/10.1016/j.ejmech.2016.04.039

 

Allegrini, F., Olivieri, A.C. Sensitivity, Prediction Uncertainty, and Detection Limit for Artificial Neural Network Calibrations (2016) Analytical Chemistry, 88 (15), pp. 7807-7812. https://doi.org/10.1021/acs.analchem.6b01857

 

Scalise, M.L., Arrúa, E.C., Rial, M.S., Esteva, M.I., Salomon, C.J., Fichera, L.E. Promising efficacy of benznidazole nanoparticles in acute trypanosoma cruzi murine model: In-vitro and in-vivo studies (2016) American Journal of Tropical Medicine and Hygiene, 95 (2), pp. 388-393. https://doi.org/10.4269/ajtmh.15-0889

 

Medran, N.S., Villalba, M., Mata, E.G., Testero, S.A. Gold-Catalyzed Cycloisomerization of Alkyne-Containing Amino Acids: Controlled Tuning of C–N vs. C–O Reactivity (2016) European Journal of Organic Chemistry, 2016 (22), pp. 3757-3764. https://doi.org/10.1002/ejoc.201600429

 

Corne, V., Sarotti, A.M., De Arellano, C.R., Spanevello, R.A., Suárez, A.G. Experimental and theoretical insights in the alkene-arene intramolecular π-stacking interaction (2016) Beilstein Journal of Organic Chemistry, 12, pp. 1616-1623. https://doi.org/10.3762/bjoc.12.158

 

Mangione, M.I., Spanevello, R.A., Minudri, D., Heredia, D., Fernandez, L., Otero, L., Fungo, F. Electropolimerization of Functionalizaed Carbazole End-Capped Dendrimers. Formation of Conductive Films (2016) Electrochimica Acta, 207, pp. 143-151. https://doi.org/10.1016/j.electacta.2016.04.154

 

Zinczuk, J., Carnavale, G.A. Synthesis of trialkyl 2-halogeno-1,1,1-ethanetricarboxylates (2016) Arkivoc, 2016 (4), pp. 352-362. https://doi.org/10.3998/ark.5550190.p009.567

 

Demicheli, V., Moreno, D.M., Jara, G.E., Lima, A., Carballal, S., Ríos, N., Batthyany, C., Ferrer-Sueta, G., Quijano, C., Estrĺn, D.A., Martí, M.A., Radi, R. Mechanism of the Reaction of Human Manganese Superoxide Dismutase with Peroxynitrite: Nitration of Critical Tyrosine 34 (2016) Biochemistry, 55 (24), pp. 3403-3417. https://doi.org/10.1021/acs.biochem.6b00045

 

Aimo, J., Promancio, E., Damiani, P.C. Determination of reducing sugars in foodstuff applying multivariate second-order calibration (2016) Analytical Methods, 8 (23), pp. 4617-4631. https://doi.org/10.1039/c6ay00964f

 

Botta, M.C., Biava, H.D., Spanevello, R.A., Mata, E.G., Suárez, A.G. Development of polymer-supported chiral aminoalcohols derived from biomass and their application to asymmetric alkylation (2016) Tetrahedron Letters, 57 (20), pp. 2186-2189. https://doi.org/10.1016/j.tetlet.2016.04.021

 

Traficante, C.I., Fagundez, C., Serra, G.L., Mata, E.G., Delpiccolo, C.M.L. Chemoselective and Sequential Palladium-Catalyzed Couplings for the Generation of Stilbene Libraries via Immobilized Substrates (2016) ACS Combinatorial Science, 18 (5), pp. 225-229. https://doi.org/10.1021/acscombsci.6b00023

 

Jäger, S.N., Mittelbach, M., Cabrera, R., Labadie, G.R. Simple method for high purity acylated steryl glucosides synthesis (2016) European Journal of Lipid Science and Technology, 118 (5), pp. 827-833. https://doi.org/10.1002/ejlt.201500205

 

Pergomet, J.L., Kaufman, T.S., Bracca, A.B.J. Expedient Approach to 6-Bromo-2-isopropylidenecoumaranone, a Potential Intermediate for the Synthesis of TMC-120B, Pseudodeflectusin, and Their Congeners (2016) Helvetica Chimica Acta, 99 (5), pp. 398-404. https://doi.org/10.1002/hlca.201500525

 

Pérez, L.M., Piccirilli, G.N., Delorenzi, N.J., Verdini, R.A. Effect of different combinations of glycerol and/or trehalose on physical and structural properties of whey protein concentrate-based edible films (2016) Food Hydrocolloids, 56, pp. 352-359. https://doi.org/10.1016/j.foodhyd.2015.12.037

 

Jäger, S.N., Porta, E.O.J., Labadie, G.R. Tuning the Lewis acid phenol ortho-prenylation as a molecular diversity tool (2016) Molecular Diversity, 20 (2), pp. 407-419. https://doi.org/10.1007/s11030-015-9644-9

 

Comba, M.B., Suárez, A.G., Sarotti, A.M., Mangione, M.I., Spanevello, R.A., Giordano, E.D.V. Synthesis of a 3-Thiomannoside (2016) Organic Letters, 18 (8), pp. 1748-1751. https://doi.org/10.1021/acs.orglett.6b00428

 

Calvo, N.L., Kaufman, T.S., Maggio, R.M. Mebendazole crystal forms in tablet formulations. An ATR-FTIR/chemometrics approach to polymorph assignment (2016) Journal of Pharmaceutical and Biomedical Analysis, 122, pp. 157-165. https://doi.org/10.1016/j.jpba.2016.01.035

 

Benítez, D., Medeiros, A., Fiestas, L., Panozzo-Zenere, E.A., Maiwald, F., Prousis, K.C., Roussaki, M., Calogeropoulou, T., Detsi, A., Jaeger, T., Šarlauskas, J., Peterlin Mašič, L., Kunick, C., Labadie, G.R., Flohé, L., Comini, M.A. Identification of Novel Chemical Scaffolds Inhibiting Trypanothione Synthetase from Pathogenic Trypanosomatids (2016) PLoS Neglected Tropical Diseases, 10 (4), art. no. e0004617. https://doi.org/10.1371/journal.pntd.0004617

 

Tomat, D., Balagué, C., Casabonne, C., Verdini, R., Quiberoni, A. Resistance of foodborne pathogen coliphages to additives applied in food manufacture (2016) LWT, 67, pp. 50-54. https://doi.org/10.1016/j.lwt.2015.11.031

 

Gómez-Caravaca, A.M., Maggio, R.M., Cerretani, L. Chemometric applications to assess quality and critical parameters of virgin and extra-virgin olive oil. A review (2016) Analytica Chimica Acta, 913, pp. 1-21. https://doi.org/10.1016/j.aca.2016.01.025

 

Luna, L.E., Forastieri, P.S., Marchiaro, P., Limansky, A., Cravero, R.M. Structural diversity and similar bioactivity in synthetic bicyclononanes (2016) Synthetic Communications, 46 (5), pp. 404-414. https://doi.org/10.1080/00397911.2016.1141429

 

Gaitano, R.O., Calvo, N.L., Narda, G.E., Kaufman, T.S., Maggio, R.M., Brusau, E.V. Preparation and Physical Characterization of a Diclofenac-Ranitidine Co-precipitate for Improving the Dissolution of Diclofenac (2016) Journal of Pharmaceutical Sciences, 105 (3), pp. 1258-1268. https://doi.org/10.1016/j.xphs.2016.01.001

 

Heredia, D.A., Larghi, E.L., Kaufman, T.S. A Straightforward Synthesis of 5-Methylaaptamine from Eugenol, Employing a 6π-Electrocyclization Reaction of a 1-Azatriene (2016) European Journal of Organic Chemistry, 2016 (7), pp. 1397-1404. https://doi.org/10.1002/ejoc.201501566

 

Blanes, P.S., Bordoni, M.E., González, J.C., García, S.I., Atria, A.M., Sala, L.F., Bellú, S.E. Application of soy hull biomass in removal of Cr(VI) from contaminated waters. Kinetic, thermodynamic and continuous sorption studies (2016) Journal of Environmental Chemical Engineering, 4 (1), pp. 516-526. https://doi.org/10.1016/j.jece.2015.12.008

 

Pérez, R.L., Escandar, G.M. Multivariate calibration-assisted high-performance liquid chromatography with dual UV and fluorimetric detection for the analysis of natural and synthetic sex hormones in environmental waters and sediments (2016) Environmental Pollution, 209, pp. 114-122. https://doi.org/10.1016/j.envpol.2015.11.024

 

Allegrini, F., Wentzell, P.D., Olivieri, A.C. Generalized error-dependent prediction uncertainty in multivariate calibration (2016) Analytica Chimica Acta, 903, pp. 51-60. https://doi.org/10.1016/j.aca.2015.11.028

 

García, A., Leonardi, D., Lamas, M.C. Promising applications in drug delivery systems of a novel β-cyclodextrin derivative obtained by green synthesis (2016) Bioorganic and Medicinal Chemistry Letters, 26 (2), pp. 602-608. https://doi.org/10.1016/j.bmcl.2015.11.067

 

Giménez, M.C., Varela, N.M., Blanes, P.S. Bioadsorption studies of arsenate from aqueous solutions using chitosan (2016) Arsenic Research and Global Sustainability – Proceedings of the 6th International Congress on Arsenic in the Environment, AS 2016, pp. 474-475. https://doi.org/10.1201/b20466-220

 

Zuljan, F., Espariz, M., Blancato, V.S., Esteban, L., Alarcón, S., Magni, C. Draft genome sequence of Lactococcus lactis subsp. lactis bv. diacetylactis CRL264, a citratefermenting strain (2016) Genome Announcements, 4 (1), art. no. e01575-15.  https://doi.org/10.1128/genomeA.01575-15

 

Grimblat, N., Sarotti, A.M., Kaufman, T.S., Simonetti, S.O. A theoretical study of the Duff reaction: Insights into its selectivity (2016) Organic and Biomolecular Chemistry, 14 (44), pp. 10496-10501. https://doi.org/10.1039/c6ob01887d

 

Carrau, G., Veiga, N., Suescun, L., Giri, G.F., Suárez, A.G., Spanevello, R., González, D. Diels–Alder reaction of two green chiral precursors. Approach to natural product like structures (2016) Tetrahedron Letters, 57 (43), pp. 4791-4794. https://doi.org/10.1016/j.tetlet.2016.09.031

 

Drusin, S.I., Suarez, I.P., Gauto, D.F., Rasia, R.M., Moreno, D.M. dsRNA-protein interactions studied by molecular dynamics techniques. Unravelling dsRNA recognition by DCL1 (2016) Archives of Biochemistry and Biophysics, 596, pp. 118-125. https://doi.org/10.1016/j.abb.2016.03.013

 

Giri, G.F., Danielli, M., Marinelli, R.A., Spanevello, R.A. Cytotoxic effect of levoglucosenone and related derivatives against human hepatocarcinoma cell lines (2016) Bioorganic and Medicinal Chemistry Letters, 26 (16), pp. 3955-3957. https://doi.org/10.1016/j.bmcl.2016.07.007

 

Padilha, G., Kaufman, T.S., Silveira, C.C. Wittig–Horner mediated synthesis of 4-vinyl sulfide derivatives of pyrazoles (2016) Tetrahedron Letters, 57 (30), pp. 3349-3353. https://doi.org/10.1016/j.tetlet.2016.06.063

 

Karak, M., Barbosa, L.C.A., Acosta, J.A.M., Sarotti, A.M., Boukouvalas, J. Thermodynamically driven,: Syn -selective vinylogous aldol reaction of tetronamides (2016) Organic and Biomolecular Chemistry, 14 (21), pp. 4897-4907. https://doi.org/10.1039/c6ob00895j

 

Simonetti, S.O., Larghi, E.L., Kaufman, T.S.Erratum: A convenient approach to an advanced intermediate toward the naturally occurring, bioactive 6-substituted 5-hydroxy-4-aryl-1H-quinolin-2-ones (2016) Organic and Biomolecular Chemistry, 14 (12), p. 3333. https://doi.org/10.1039/c6ob90030e

 

Grimblat, N., Sarotti, A.M., Pisano, P.L., Pellegrinet, S.C. α-Hydroxyacids accelerate the Diels-Alder reaction of dibutyl vinylboronate with cyclopentadiene: Experimental results and mechanistic insights (2016) New Journal of Chemistry, 40 (3), pp. 1966-1969. https://doi.org/10.1039/c5nj03015c

 

Simonetti, S.O., Larghi, E.L., Kaufman, T.S. A convenient approach to an advanced intermediate toward the naturally occurring, bioactive 6-substituted 5-hydroxy-4-aryl-1H-quinolin-2-ones (2016) Organic and Biomolecular Chemistry, 14 (9), pp. 2625-2636. https://doi.org/10.1039/c5ob02680f

 

Rudroff, F., Bianchi, D.A., Moran-Ramallal, R., Iqbal, N., Dreier, D., Mihovilovic, M.D. Synthesis of tetrahydrofuran-based natural products and their carba analogs via stereoselective enzyme mediated Baeyer–Villiger oxidation (2016) Tetrahedron, 72 (46), pp. 7212-7221. https://doi.org/10.1016/j.tet.2015.11.048

2015

Arrúa, E.C., Ferreira, M.J.G., Salomon, C.J., Nunes, T.G. Elucidating the guest-host interactions and complex formation of praziquantel and cyclodextrin derivatives by 13C and 15N solid-state NMR spectroscopy (2015) International Journal of Pharmaceutics, 496 (2), pp. 812-821. https://doi.org/10.1016/j.ijpharm.2015.11.026

 

Signorella, S., Daier, V., Ledesma, G., Palopoli, C., Back, D.F., Lang, E.S., Kopp, C.R., Ebani, P., Pereira, M.B., Giacomelli, C., Piquini, P.C. Synthesis, structure and SOD activity of Mn complexes with symmetric Schiff base ligands derived from pyridoxal (2015) Polyhedron, 102, pp. 176-184. https://doi.org/10.1016/j.poly.2015.09.007

 

Grimblat, N., Zanardi, M.M., Sarotti, A.M. Beyond DP4: An Improved Probability for the Stereochemical Assignment of Isomeric Compounds using Quantum Chemical Calculations of NMR Shifts (2015) Journal of Organic Chemistry, 80 (24), pp. 12526-12534. https://doi.org/10.1021/acs.joc.5b02396

 

Bravo, M.A., Escandar, G.M., Olivieri, A.C., Bardin, E., Aguilar, L.F., Quiroz, W. A novel application of nylon membranes for tributyltin determination in complex environmental samples by fluorescence spectroscopy and multivariate calibration (2015) Chemometrics and Intelligent Laboratory Systems, 148, pp. 77-84. https://doi.org/10.1016/j.chemolab.2015.09.005

 

Moreno-Sastre, M., Pastor, M., Salomon, C.J., Esquisabel, A., Pedraz, J.L. Pulmonary drug delivery: A review on nanocarriers for antibacterial chemotherapy (2015) Journal of Antimicrobial Chemotherapy, 70 (11), pp. 2945-2955. https://doi.org/10.1093/jac/dkv192

 

Navarro-Reig, M., Jaumot, J., García-Reiriz, A., Tauler, R. Evaluation of changes induced in rice metabolome by Cd and Cu exposure using LC-MS with XCMS and MCR-ALS data analysis strategies (2015) Analytical and Bioanalytical Chemistry, 407 (29), pp. 8835-8847. https://doi.org/10.1007/s00216-015-9042-2

 

Coronel, A.C., Zinczuk, J., Fernández, L.E., Varetti, E.L. An experimental and theoretical vibrational study of 3,3,6,6-tetramethyl-1,2,4,5-tetrathiane (2015) Vibrational Spectroscopy, 81, pp. 40-45. https://doi.org/10.1016/j.vibspec.2015.09.006

 

Novaes, L.F.T., Sarotti, A.M., Pilli, R.A. Total Synthesis and Tentative Structural Elucidation of Cryptomoscatone E3: Interplay of Experimental and Computational Studies (2015) Journal of Organic Chemistry, 80 (24), pp. 12027-12037. https://doi.org/10.1021/acs.joc.5b01956

 

Giri, G.F., Sarotti, A.M., Spanevello, R.A. Understanding reactivity and regioselectivity in Diels-Alder reactions of a sugar-derived dienophile bearing two competing EWGs. An experimental and computational study (2015) Carbohydrate Research, 415, art. no. 7043, pp. 54-59. https://doi.org/10.1016/j.carres.2015.07.017

 

Zanardi, M.M., Sarotti, A.M. GIAO C-H COSY Simulations Merged with Artificial Neural Networks Pattern Recognition Analysis. Pushing the Structural Validation a Step Forward (2015) Journal of Organic Chemistry, 80 (19), pp. 9371-9378. https://doi.org/10.1021/acs.joc.5b01663

 

Martins, G.M., Zeni, G., Back, D.F., Kaufman, T.S., Silveira, C.C. Expedient Iodocyclization Approach Toward Polysubstituted 3H-Benzo[e]indoles (2015) Advanced Synthesis and Catalysis, 357 (14-15), pp. 3255-3261. https://doi.org/10.1002/adsc.201500275

 

Soazo, M., Báez, G., Barboza, A., Busti, P.A., Rubiolo, A., Verdini, R., Delorenzi, N.J. Heat treatment of calcium alginate films obtained by ultrasonic atomizing: Physicochemical characterization (2015) Food Hydrocolloids, 51, pp. 193-199. https://doi.org/10.1016/j.foodhyd.2015.04.037

 

Vallejos, M.M., Pellegrinet, S.C. Competing mechanisms for the reaction of dichloropropynylborane with 2-tert-butylbutadiene. Diels-Alder reaction versus alkynylboration (2015) RSC Advances, 5 (86), pp. 70147-70155. https://doi.org/10.1039/c5ra12903f

 

Brito, G.A., Sarotti, A.M., Wipf, P., Pilli, R.A. Cascade cyclization triggered by imine formation. Formal synthesis of the alkaloid (±)-stemoamide and its 9a-epimer (2015) Tetrahedron Letters, 56 (48), pp. 6664-6668. https://doi.org/10.1016/j.tetlet.2015.10.017

 

Riveira, M.J., Trigo-Mouriño, P., Troche-Pesqueira, E., Martin, G.E., Navarro-Vázquez, A., Mischne, M.P., Gil, R.R. Self-Sensitized Photooxygenation of 2H-Pyrans: Characterization of Unexpected Products Assisted by Computed Structural Elucidation and Residual Dipolar Couplings (2015) Journal of Organic Chemistry, 80 (15), pp. 7396-7402. https://doi.org/10.1021/acs.joc.5b00817

 

Gerosa, G.G., Spanevello, R.A., Suárez, A.G., Sarotti, A.M. Joint Experimental, in Silico, and NMR Studies toward the Rational Design of Iminium-Based Organocatalyst Derived from Renewable Sources (2015) Journal of Organic Chemistry, 80 (15), pp. 7626-7634.  https://doi.org/10.1021/acs.joc.5b01214

 

Padrõ, J.M., Osorio-Grisales, J., Arancibia, J.A., Olivieri, A.C., Castells, C.B. Scope of partial least-squares regression applied to the enantiomeric composition determination of ketoprofen from strongly overlapped chromatographic profiles (2015) Journal of Separation Science, 38 (14), pp. 2423-2430. https://doi.org/10.1002/jssc.201500217

 

Luna, L.E., Tontarelli, W., Forastieri, P., Cravero, R.M. Novel Cyclic Enaminone Esters and N-Heterocycles by Divergent Chemical Behavior through Amine-Mediated Reactions (2015) Helvetica Chimica Acta, 98 (7), pp. 994-1003. https://doi.org/10.1002/hlca.201400376

 

Priotti, J., Ferreira, M.J.G., Lamas, M.C., Leonardi, D., Salomon, C.J., Nunes, T.G. First solid-state NMR spectroscopy evaluation of complexes of benznidazole with cyclodextrin derivatives (2015) Carbohydrate Polymers, 131, pp. 90-97. https://doi.org/10.1016/j.carbpol.2015.05.045

 

Riveira, M.J., Quiroga, G.N., Mata, E.G., Gandon, V., Mischne, M.P. Cycloisomerization of Conjugated Trienones and Isomeric 2 H -Pyrans: Unified Strategy toward Cyclopenta[ b ]furans (2015) Journal of Organic Chemistry, 80 (12), pp. 6515-6519. https://doi.org/10.1021/acs.joc.5b00818

 

Vidal, R.B.P., Ibañez, G.A., Escandar, G.M. Chemometrics-assisted cyclodextrin-enhanced excitation-emission fluorescence spectroscopy for the simultaneous green determination of bisphenol A and nonylphenol in plastics (2015) Talanta, 143, art. no. 15622, pp. 162-168. https://doi.org/10.1016/j.talanta.2015.05.030

 

Ferreira, M.J.G., García, A., Leonardi, D., Salomon, C.J., Lamas, M.C., Nunes, T.G. 13C and 15N solid-state NMR studies on albendazole and cyclodextrin albendazole complexes (2015) Carbohydrate Polymers, 123, pp. 130-135. https://doi.org/10.1016/j.carbpol.2015.01.031

 

Codina, A.V., García, A., Leonardi, D., Vasconi, M.D., Di Masso, R.J., Lamas, M.C., Hinrichsen, L.I. Efficacy of albendazole:β-cyclodextrin citrate in the parenteral stage of Trichinella spiralis infection (2015) International Journal of Biological Macromolecules, 77, pp. 203-206. https://doi.org/10.1016/j.ijbiomac.2015.02.049

 

Larghi, E.L., Bracca, A.B.J., Aguilar, A.A.A., Heredia, D.A., Pergomet, J.L., Simonetti, S.O., Kaufman, T.S.Neocryptolepine: A promising indoloisoquinoline alkaloid with interesting biological activity. Evaluation of the drug and its most relevant analogs (2015) Current Topics in Medicinal Chemistry, 15 (17), pp. 1683-1707. https://doi.org/10.2174/1568026615666150427113937

 

Kaufman, T.S. The multiple faces of Eugenol. A versatile starting material and building block for organic and bio-organic synthesis and a convenient precursor toward bio-based fine chemicals (2015) Journal of the Brazilian Chemical Society, 26 (6), pp. 1055-1085.  https://doi.org/10.5935/0103-5053.20150086

 

Zanardi, M.M., Suárez, A.G. Synthesis of new chiral 1,3-aminoalcohols derived from levoglucosenone and their application in asymmetric alkylations (2015) Tetrahedron Letters, 56 (24), pp. 3762-3765. https://doi.org/10.1016/j.tetlet.2015.04.051

 

Calvo, N.L., Simonetti, S.O., Maggio, R.M., Kaufman, T.S. Thermally induced solid-state transformation of cimetidine. A multi-spectroscopic/chemometrics determination of the kinetics of the process and structural elucidation of one of the products as a stable N3-enamino tautomer (2015) Analytica Chimica Acta, 875, pp. 22-32. https://doi.org/10.1016/j.aca.2015.02.033

 

Pisano, P.L., Silva, M.F., Olivieri, A.C. Anthocyanins as markers for the classification of Argentinean wines according to botanical and geographical origin. Chemometric modeling of liquid chromatography-mass spectrometry data (2015) Food Chemistry, 175, pp. 174-180. https://doi.org/10.1016/j.foodchem.2014.11.124

 

Ruckebusch, C., Bernex, R., Allegrini, F., Sliwa, M., Hofkens, J., Dedecker, P. Mapping pixel dissimilarity in wide-field super-resolution fluorescence microscopy (2015) Analytical Chemistry, 87 (9), pp. 4675-4682. https://doi.org/10.1021/ac504295p

 

Olivieri, A.C. Practical guidelines for reporting results in single- and multi-component analytical calibration: A tutorial (2015) Analytica Chimica Acta, 868, pp. 10-22. https://doi.org/10.1016/j.aca.2015.01.017

 

Ledesma, J., Bortolato, S.A., Martino, D.M., Boschetti, C.E. Fluorescence spectroscopy and multivariate analysis as a greener monitoring tool: characterization of the curing kinetics of bioinspired polymers (2015) Green Chemistry Letters and Reviews, 8 (2), pp. 26-38. https://doi.org/10.1080/17518253.2015.1073798

 

Boggián, D.B., Cornier, P.G., Mata, E.G., Blank, V.C., Cárdenas, M.G., Roguin, L.P. A solid- and solution-phase-based library of 2β-methyl substituted penicillin derivatives and their effects on growth inhibition of tumor cell lines (2015) MedChemComm, 6 (4), pp. 619-625. https://doi.org/10.1039/c4md00430b

 

Vignaduzzo, S.E., Operto, M.A., Castellano, P.M. Development and validation of a dissolution test method for albendazole and praziquantel in their combined dosage form (2015) Journal of the Brazilian Chemical Society, 26 (4), pp. 729-735. https://doi.org/10.5935/0103-5053.20150033

 

Calvo, N.L., Kaufman, T.S., Maggio, R.M. A PCA-based chemometrics-assisted ATR-FTIR approach for the classification of polymorphs of cimetidine: Application to physical mixtures and tablets (2015) Journal of Pharmaceutical and Biomedical Analysis, 107, pp. 419-425.  https://doi.org/10.1016/j.jpba.2015.01.016

 

Soazo, M., Pérez, L.M., Rubiolo, A.C., Verdini, R.A. Prefreezing application of whey protein-based edible coating to maintain quality attributes of strawberries (2015) International Journal of Food Science and Technology, 50 (3), pp. 605-611. https://doi.org/10.1111/ijfs.12667

 

Méndez, L., Mata, E.G. Solid-supported cross-metathesis and a formal alkane metathesis for the generation of biologically relevant molecules (2015) ACS Combinatorial Science, 17 (2), pp. 81-86. https://doi.org/10.1021/co500176b

 

Bortolato, S.A., Lozano, V.A., de la Peña, A.M., Olivieri, A.C. Novel augmented parallel factor model for four-way calibration of high-performance liquid chromatography-fluorescence excitation-emission data (2015) Chemometrics and Intelligent Laboratory Systems, 141, pp. 1-11. https://doi.org/10.1016/j.chemolab.2014.11.013

 

García, A., Leonardi, D., Piccirilli, G.N., Mamprin, M.E., Olivieri, A.C., Lamas, M.C. Spray drying formulation of albendazole microspheres by experimental design. In vitro – In vivo studies (2015) Drug Development and Industrial Pharmacy, 41 (2), pp. 244-252. https://doi.org/10.3109/03639045.2013.858737

 

Zurita, M.A., Avila, A., Spanevello, R.A., Suárez, A.G., Sarotti, A.M. Montmorillonite K-10 promoted synthesis of chiral dioxa-caged compounds derived from levoglucosenone (2015) Carbohydrate Research, 402, pp. 67-70. https://doi.org/10.1016/j.carres.2014.07.019

 

Mangione, M.I., Spanevello, R.A. Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction (2015) Tetrahedron Letters, 56 (2), pp. 465-467. https://doi.org/10.1016/j.tetlet.2014.11.133

 

Castillo, M.V., Pergomet, J.L., Carnavale, G.A., Davies, L., Zinczuk, J., Brandán, S.A. A complete vibrational study on a potential environmental toxicant agent, the 3,3′,4,4′-tetrachloroazobenzene combining the FTIR, FTRaman, UV-Visible and NMR spectroscopies with DFT calculations (2015) Spectrochimica Acta – Part A: Molecular and Biomolecular Spectroscopy, 134, pp. 577-586. https://doi.org/10.1016/j.saa.2014.07.032

 

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Simonetti, S.O., Larghi, E.L., Kaufman, T.S. Alternate and step-economic synthesis of the β-Methylstyrene chelating pre-ligand of the Hoveyda-Grubbs II catalyst (2015) Organic Preparations and Procedures International, 47 (3), pp. 227-231. https://doi.org/10.1080/00304948.2015.1025021

 

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Traficante, C.I., Mata, E.G., Delpiccolo, C.M.L. Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling. the role of water and copper(I) salts (2015) RSC Advances, 5 (34), pp. 26796-26800. https://doi.org/10.1039/c5ra03732h

 

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Bassaco, M.M., Fortes, M.P., Kaufman, T.S., Silveira, C.C. Metal-free synthesis of 3,5-disubstituted 1H- and 1-aryl-1H-pyrazoles from 1,3-diyne-indole derivatives employing two successive hydroaminations (2015) RSC Advances, 5 (27), pp. 21112-21124. https://doi.org/10.1039/c4ra16439c

 

Pellegrino Vidal, R.B., Ibañez, G.A., Escandar, G.M. Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrin media (2015) RSC Advances, 5 (27), pp. 20914-20923.   https://doi.org/10.1039/c4ra13023e

 

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